International Journal of Medical and Pharmaceutical Research
2025, Volume-6, Issue-5 : 497-504
Research Article
Comparison OF IV Dexmedetomidine and IV Esmolol for Suppression of Hemodynamic Response to Laryngoscopy and Endotracheal Intubation
 ,
 ,
 ,
 ,
Received
Aug. 10, 2025
Accepted
Aug. 31, 2025
Published
Sept. 18, 2025
Abstract

Background: Direct laryngoscopy and endotracheal intubation are almost always associated with hemodynamic changes such as hypertension, tachycardia and arrhythmias[1,8,13].The purpose of our study was to compare intravenous Dexmedetomidine(1mcg/kg) and intravenous Esmolol(1.5 mg/kg) for suppression of hemodynamic

responses secondary to laryngoscopy and endotracheal intubation.

Material and methods: This was a comparative, observational, and prospective study in which total 60 patients undergoing elective  surgery under general anaesthesia were divided into two equal groups. Group-D received inj. Dexmedetomidine 1 mcg/kg IV infusion (diluted to 10 ml with normal saline) over 10 minutes before induction

Group E: Patients who received Injection Esmolol 1.5 mg/Kg IV (diluted to 10 ml with normal saline) 2 minutes before induction. Baseline preoperative values of hemodynamic parameters were recorded. Both groups were observed for  Changes in HR,SBP,DBP,MAP and Spo2,After study drug, After induction, Immediately after intubation,At 1 min, 3 min, 5 min, 7 min, 10 min after Intubation and Patients were observed for any adverse effects and treated accordingly.

Result:From the observation it was found that Dexmedetomidine had better attenuation of the stress response during laryngoscopy and intubation than Esmolol. However, there was no significant difference in hemodynamic parameters after study drug and after induction,there was highly significant difference between two groups immediately after intubation and 1,3,5,7,10 min after intubation.

Conclusion: Dexmedetomidine 1 mcg/kg IV was more effective in attenuating the hemodynamic stress response to laryngoscopy and intubation, provides more hemodynamic stability as compared Esmolol 1.5 mg/kg IV.

Keywords
INTRODUCTION

Laryngoscopy and endotracheal intubation are commonly performed procedures in anaesthesia and critical care settings. Direct laryngoscopy and endotracheal intubation are almost always associated with hemodynamic changes such as hypertension, tachycardia and arrhythmias[1,8,13]. In 1940 Reid and Brace [10] studied the reflex effect upon the heart during irritation of the respiratory tract which lead to reflex sympathetic stimulation and described that this reflex is due to provocation of larynx and pharynx. The response is transient and occurs 30 seconds after intubation and last for less than 10 minutes. Hypertension and tachycardia may predispose an individual to development of pulmonary edema[3],myocardial insufficiency and raised intracranial pressure especially in patients with is chaemic heart disease, cerebrovascular disease, hypertension, old age, and diabetes mellitus. Hemodynamic stability is the most essential goal of anaesthetic management plan. There are various methods and drugs[9] used to reduce this pressor response to laryngoscopy and endotracheal intubation.

 

Perioperative beta-blocker use in cardiac surgery by Blessbergeretal[2]have shown beneficial effects as they reduce rhythm disturbances. Esmolol is a cardio selective,ultra short acting,beta blocking agent with short half life(9min). It blocks the beta adrenergic receptors and also reduces the force of contraction and heart rate[7].This agent has been used to reduce the hemodynamic response to laryngoscopy and intubation.

 

Dexmedetomidine is an imidazole derivative and selective alpha-2 adrenergic receptor agonist which produces hyperpolarization of noradrenergic neurons and suppression of neuronal firing in the locus ceruleus leading to decreased systemic noradrenaline release and causing attenuation of sympathoadrenal responses and hemodynamic stability during laryngoscopy and tracheal intubation[4] The effects of dexmedetomidine include anxiolysis,sedation, analgesia and sympatholysis with minimal or no respiratory depression[12]The purpose of our study was to compare intravenous Dexmedetomidine(1mcg/kg) and intravenous Esmolol(1.5 mg/kg) for suppression of hemodynamic responses secondary to laryngoscopy and endotracheal intubation.

 

AIMS AND OBJECTIVE

The aim of the present study was to compare the efficacy of intravenous Dexmedetomidine (1 mcg/kg) and Esmolol (1.5 mg/kg) for suppression of hemodynamic response to laryngoscopy and endotracheal intubation in patients undergoing elective surgery under general anaesthesia.

 

THE OBJECTIVES OF THE STUDY ARE

To compare haemodynamic response in terms of Heart rate,Systolic blood pressure,Diastolic blood pressure,Mean arterial pressure,Oxygensaturation,To observe for any adverse effect

 

MATERIALS AND METHODS

Study design:This was a comparative, observational, and prospective study conducted in SVP Hospital, NHL Municipal Medical College, Ahmedabad, India. After receiving an approval letter from ethical committee of the institute, 60 patients planned for the elective  surgery under general anaesthesia were enlisted in the study.

 

The sample size was obtained based on previous studies.

 

Inclusion Criteria

Patients between 20 to 50 years  age group both gender, ASA grade of I / II posted for elective surgeries under general anaesthesia

 

Exclusion criteria

This study excluded patients less than 20 years and more than 50 years of age,Patientsrefusal,Patient with ASA(American society of anaesthesiologist) class above II Patients known to have drug allergies ,Predicted difficult intubation Intubation time more than 30sec or intubation in more than 1 attempt Patients on treatment with beta blocker or calcium channel blocker drugs Patients with comorbidities like uncontrolled diabetes mellitus, coronary artery disease, cardiovascular disease,Pregnant women.

 

INFORMED CONSENT: written and informed consent will be obtained.

 

STUDY PROCEDURE :

Patients fulfilling the inclusion criteria The nature of study and procedure will be explained to the patient and written informed consent was taken, Each patient was assessed preoperatively by General andsystemic examination.All the patients in this study received general anaesthesia as per routine protocol of the institute by the consultant anaesthesiologist of the hospital and all the parameters were observed and noted.All the patients will go for routine pre-anesthetic checkup with necessary  investigations.

 

Preoperative preparation:Anesthetictrolly and emergency drug tray checked.Pre operative pulse, blood pressure, spo2 will be recorded.After establishing intravenous access, an infusion of intravenous fluids will be started.All patients will be receiving inj. Glycopyrrolate(0.004mg/kg) iv and injondansetron(0.15mg/kg )iv as premedication.

 

GROUP D Receive I.V Dexmedetomidine 1 mcg/kg over 10 minutes before intubation.

 

GROUP E Receive I.V Esmolol 1.5 mg/kg over 2 minutes before intubation.

 

Preoxygenation will be done with 100% oxygen for 3 minutes.

Induction will be done by Inj. Thiopentone(6 mg/kg) iv followed by inj. succinylcholine(2 mg/kg) iv.

Endotracheal intubation will be done by appropriate size oral,portex,cuffed,endotrachealtube.bilateral air entry checked,present,equal,tube fixed. Maintenance of anesthesia will be carried out with 50% O2 and 50% N2O + sevoflurane + inj.atracurium 0.5mg/kg iv loading dose and 0.1mg/kg iv in maintenance doses.

 

At the end of surgery residual neuromuscular blockade will be reversed by appropriate  doses of Inj. glycopyrrolate(0.008 mg/kg) and neostigmine (0.05 mg/kg)

 

Extubation will be carried out after returns of smooth respiration,good muscle tone and  power,eye opening and all protective reflexes.

 

Observations

THE FOLLOWING PARAMETERS WILL BE COMPARED BETWEEN 2 GROUPS: The blood pressure, heart rate,spo2  will be recorded at baseline,after study drug,after induction ,immediately after intubation,1,3,5,7,10 minutes after intubation

 

Statistical analysis

Statistical analysis was done by using descriptive and inferential statistics using Chi-square test and students unpaired t test to find out the significance of various study parameters among the two groups with a significance threshold set at ‘p’ value <0.05.

 

Observations and RESULTS Total sixty patients who fulfilled inclusion criteria were selected for the study and according the given study drugs,they were allocated to groups. Changes in HR,SBP,DBP,MAP and Spo2 were recorded at baseline,after study drug,afterinduction,immediately after intubation and 1,3,5,7,10 minutes after intubation.

 

(1)    DEMOGRAPHIC DATA

 

TABLE:1

Demographic data

Patient Data

GROUP E

GROUP D

P value

Inference

Number Of Patients

30

30

-

 

Age( years)

36.03 ±8.80

36.3 ±7.82

0.90

NS

Male:Female

14:16

16:14

-

-

Weight (kgs)

57.7 ±5.98

57.6 ±6.61

0.92

NS

ASA

Grade

I

14

15

-

-

II

16

15

 

Table-1 Compares the demographic characteristics of all the patients which were clinically comparable among both the groups(P Value>0.05).Patients belonging to ASA grade I and II were included in this study.

 

TABLE 2 shows the distribution of the patients according to the type of surgeries in both the groups.

DISTRIBUTION ACCORDING TO TYPE OF SURGERY

TYPE OF SURGERY

GROUP E

GROUP D

No. of

Patients

%

No. of

Patients

%

General Surgery

14

46.66%

15

50%

ENT Surgery

5

16.66%

4

13.33%

Gynaecological Surgery

5

16.66%

6

20%

Orthopaedic Surgery

6

20%

5

16.66%

 

Table 2: Table shows the distribution of the patients according to the type of surgeries in both the groups.

 
   

 

Graph 1 : Shows the age distribution amongst both the groups.

Graph 2 : Shows the sex distribution amongst both the groups.

Graph 3 : Shows the weight distribution amongst both the groups.

Graph 4: Shows the distribution according to the types of surgeries amongst both the groups.

 

In This study of 60 patients,29 patients were posted for general surgery,9 patients were posted for ent surgery,11 were posted for gynaecological surgery and 11 patients were posted for orthopedic surgery.

 

(2)  HEART RATE

The heart rate is measured at baseline,after study drug,afterinduction,immediately after intubation, 1,3,5,7,10 minutes after intubation (Table 3, Graph 5).TABLE-3: CHANGES IN HEART RATE

 

CHANGES IN HEART RATE (bpm)

TIME

GROUP E

GROUP D

P VALUE

Inference

MEAN

SD

MEAN

SD

Baseline

83.27

4.71

84.93

5.42

0.21

NS

After study drug

80.60

5.31

79.30

7.98

0.46

NS

After induction

79.60

5.10

77.33

4.01

0.08

NS

Immediately after intubation

91.47

3.36

85.67

4.79

<0.001

HS

I+ 1

94.07

3.50

87.93

4.65

<0.001

HS

I+ 3

89.00

4.03

84.63

4.48

<0.001

HS

I+ 5

84.20

4.05

78.33

4.30

<0.001

HS

I+ 7

83.07

4.89

74.73

4.78

<0.001

HS

I+ 10

81.33

5.29

71.00

4.54

<0.001

HS

 

 

The HR at baseline ,after study drug and after induction was comparable in both the group and there was no significant difference between the two groups (P Value >0.05)

 

At Immediately after intubation and 1,3,5,7 and 10 minutes after intubation  ,HR difference was statistically highly significant between the two groups (P Value<0.001).         

 

GRAPH 5:HEART RATE IN BOTH GROUPS AT VARIOUS TIME INTERVALS

 

(3)           SYSTOLIC BLOOD PRESSURE

The systolic blood pressure was measured at baseline,after study drug,afterinduction,immediately after intubation, 1,3,5,7,10 min after intubation(Table 4, Graph 6).

 

TABLE 4: CHANGES IN SYSTOLIC BLOOD PRESSURE

CHANGES IN SYSTOLIC BLOOD PRESSURE(mmhg)

TIME

GROUP E

GROUP D

P VALUE

Inference

MEAN

SD

MEAN

SD

Baseline

121.93

6.78

124.33

4.27

0.11

NS

After study drug

119.33

5.76

118.33

5.44

0.49

NS

After induction

117.33

5.47

116.80

5.60

0.71

NS

Immediately after intubation

133.73

3.43

125.00

5.32

<0.001

HS

I+ 1

136.20

3.17

127.40

5.38

<0.001

HS

I+ 3

131.00

4.09

124.60

5.41

<0.001

HS

I+ 5

126.73

4.77

119.87

4.41

<0.001

HS

I+ 7

123.87

4.78

116.73

3.98

<0.001

HS

I+ 10

122.73

4.22

114.80

4.16

<0.001

HS

 

The SBP at baseline,after study drug and after induction was comparable in both the groups and there was statistically no significant difference between the two groups (P Value >0.05).

 

At Immediately after intubation and 1,3,5,7 and 10 minutes after intubation  ,SBP difference was statistically highly significant between the two groups (P Value<0.001).

GRAPH 6: SBP IN BOTH GROUPS AT VARIOUS TIME INTERVALS

 

(4)           DIASTOLIC BLOOD PRESSURE

The Diastolic Blood Pressure was measured at baseline, After Study Drug,After induction, After intubation, at 1,3,5,7,10 min after intubation (Table 5, Graph 7).

 

TABLE 5: CHANGES IN DIASTOLIC BLOOD PRESSURE

CHANGES IN DIASTOLIC BLOOD PRESSURE (mmhg)

TIME

GROUP E

GROUP D

P VALUE

Inference

MEAN

SD

MEAN

SD

Baseline

77.80

5.95

79.83

4.70

0.14

NS

After study drug

76.40

4.83

75.93

4.43

0.69

NS

After induction

72.07

4.94

72.27

5.11

0.88

NS

Immediately after intubation

87.80

3.50

81.93

4.53

<0.001

HS

I+ 1

90.13

3.48

83.87

4.55

<0.001

HS

I+ 3

84.47

3.59

77.90

4.47

<0.001

HS

I+ 5

77.93

3.88

73.57

4.06

<0.001

HS

I+ 7

75.60

3.54

70.73

3.89

<0.001

HS

I+ 10

73.73

3.55

68.73

3.58

<0.001

HS

The DBP at baseline,after study drug and after induction was comparable in both the groups and there was statistically no significant difference between the two groups (P Value >0.05)

 

At Immediately after intubation and 1,3, 5 ,7, 10 minutes after intubation ,DBP difference was statistically highly significant between the two groups(P Value <0.001).

 

GRAPH 7: DBP IN BOTH GROUPS AT VARIOUS TIME INTERVALS

 

(5)           MEAN ARTERIAL PRESSURE

The Mean Arterial Pressure was measured at baseline, before induction, at intubation, at 1,3,5,7,10 min after intubation (Table 6, Graph 8).

 

TABLE 6: CHANGES IN MEAN ARTERIAL PRESSURE

CHANGES IN MEAN ARTERIAL BLOOD PRESSURE (mmhg)

TIME

GROUP E

GROUP D

P VALUE

Inference

MEAN

SD

MEAN

SD

Baseline

92.51

4.90

94.67

3.79

0.06

NS

After study drug

90.71

4.10

90.07

3.98

0.54

NS

After induction

87.16

4.25

87.11

4.48

0.97

NS

Immediately after intubation

103.11

2.80

96.29

3.87

<0.001

HS

I+ 1

105.49

2.80

98.38

3.95

<0.001

HS

I+ 3

99.98

2.98

93.47

4.10

<0.001

HS

I+ 5

94.20

2.79

89.00

3.64

<0.001

HS

I+ 7

91.69

3.02

86.07

3.51

<0.001

HS

I+ 10

90.07

3.10

84.09

3.21

<0.001

HS

 

The MAP at baseline,after study drug and after induction was comparable in both the groups and there was statistically no significant difference between the two groups (P Value >0.05) At Immediately after intubation and 1,3, 5 ,7, 10 minutes after intubation ,MAP difference was statistically highly significant between the two groups(P Value <0.001).

 

.

GRAPH 8: MAP IN BOTH GROUPS AT VARIOUS TIME INTERVAL

 

(6)           SPO2

SPO2 was measured at baseline, After Study Drug,After induction, After intubation, at 1,3,5,7,10 min after intubation (Table 7, Graph 9).TABLE 7: CHANGES IN SPO2

SPO2

GROUP E

GROUP D

P Value

MEAN

SD

MEAN

SD

Baseline

99.27

0.64

99.5

0.51

>0.05

After study drug

99.03

0.76

98.8

0.61

>0.05

After induction

99.27

0.69

99.53

0.51

>0.05

Immediately after

intubation

99.4

0.62

99.63

0.49

>0.05

I+ 1

99.07

0.64

98.97

0.76

>0.05

I+ 3

99.13

0.68

98.87

0.68

>0.05

I+ 5

99.43

0.63

99.63

0.49

>0.05

I+ 7

99.33

0.76

99.57

0.50

>0.05

I+ 10

99.2

0.48

99.17

0.83

>0.05

 

SPO2 In both Group at baseline, After Study Drug,After induction, After intubation, at 1,3,5,7,10 min after intubation was comparable to each other as there is no statistically significant difference between them P value( >0.05)

 

TABLE OF ADVERSE EFFECTS

Perioperative complications

Group E (n=30)

No.ofpatients(%)

Group D (n=30)

No.ofpatients(%)

Bradycardia

—----

1(3.33%)

Tachycardia

—----

—----

Arrhythmia

—----

—----

Hypertension

—----

—----

Hypotension

—----

—----

Sedation

—----

—----

Vomiting

—----

—----

In our study, one patient in Group D has bradycardia and treated with injection atropine 0.6 mg IV.

 

DISCUSSION

Laryngoscopy and endotracheal intubation have become an integral part of anaesthetic management and critical care since their description in 1921 by Rowbotham and Magill[10].Circulatory response to laryngeal and tracheal stimulation in the form of tachycardia, hypertension and dysrhythmia was known since 1940[10,11]. The principal behind the hypertension and tachycardia is the exaggerated sympathetic action due to increased catecholamine release[5].The increase in HR and blood pressure is usually transient,variable and unpredictable.It may not be of much significant in healthy individuals,but can be hazardous in those with hypertension,cardiacdysfunction,coronary artery disease or cerebrovascular disease[3]

 

Esmolol is a cardioselective beta-1 antagonist,without any intrinsic sympathomimetic effect or membrane stabilising property. And onset of action within a minute produces hemodynamic stability soon after its administration.its action is similar to other b-blockers,decreasing cardiac output by reducing heart rate and force of contraction,cardiac work and oxygen consumption are reduced.IN 1990 PARNASS SM,KERCHBERGER JP et al[6] demonstrated that single bolus dose of esmolol blunted tachycardia and hypertensive response to laryngoscopy and endotracheal intubation.

 

Dexmedetomidine is a newer alpha-2 agonist having 8-times more affinity for alpha-2 adrenoceptors as compared with Clonidine. It acts by inhibition of sympathetic outflow as well as stimulation of pre synaptic alpha 2 receptors , causing a decrease in norepinephrine release, resulting in fall in blood pressure and heart rate. Dexmedetomidine offers a unique pharmacological profile with sedation, sympatholysis, analgesia, opioid and anaesthetic sparing effect, cardiovascular stability and with great advantage to avoid respiratory depression.

 

The present study was conducted to evaluate and compare the efficacy of intravenous Esmolol and Dexmedetomidine in attenuation of hemodynamic response to laryngoscopy and endotracheal intubation. Sixty patients aged 20-50 years of either sex belonging to ASA grade I or II undergoing elective surgery under general anaesthesia were selected and divided in two groups of 30 patients each.

Group D: Patients received Injection Dexmedetomidine 1 mcg/kg IV infusion (diluted to 10 ml with normal saline) over 10 minutes before induction.

Group E: Patients received Injection Esmolol Hydrochloride 1.5 mg/Kg IV ( diluted to 10 ml with normal saline) 2 minutes before induction.

 

CONCLUSION

The findings of present study suggest that Dexmedetomidine 1 mcg/kg IV was more effective in attenuating the hemodynamic stress response to laryngoscopy and intubation,provides more hemodynamic stability as compared to Esmolol 1.5 mg/kg IV.

 

Source of Support: Nil

Conflict of Interest: None Declared

 

BIBLIOGRAPHY

  1. Barak M, Ziser A, Greenberg A, Lischinsky S, Rosenberg B. Haemodynamic and catecholamine response to tracheal intubation: Direct laryngoscopy compared with fiberoptic intubation. J ClinAnesth 2003;15:132-6
  2. Blessberger H, Kammler J, Domanovits H, Schlager O, Wildner B, Azar D, et al. Perioperative beta-blockers for preventing surgery-related mortality and morbidity. Cochrane Database Syst Rev. 2018;3:CD004476.[PMCID PMC6494407] [PubMed: 29533470]
  3. Fox, E.J., Sklar, G.S., Hill, C.H., Villanueva, R., & King, B.D. (1977). Complications related to the pressor response to endotracheal intubation. Anaesthesiology, 47, 524-525.
  4. Grewal A. Dexmedetomidine: new avenues. J AnaesthesiolClinPharmacol. 2011;27:297-302.
  5. Kovac AL. Controlling the haemodynamic response to laryngoscopy and endotracheal intubation. J Clinical Anaesth 1996;8(1):63-79.
  6. S.M., Rothenberg D.M, Kerchberger J.P. and Ivankovich AD-A single bolus dose of esmolol in the prevention of intubation – induced tachycardia and hypertension. Journal of Clinical Anaesthesia (1990) July-Aug2(4):232-237.22.
  7. Parvez G, Ommid M, Gupta AK, Heena H, Hasiha AH. Attenuation of pressor response to laryngoscopy and tracheal intubation with intravenous diltiazem and esmolol intravenous in controlled hypertensive surgical patients. Rev ColombAnesthesiol. 2010;38:457–69.
  8. Prys-Roberts C, Greene LT, Meloche R, Foëx P. Studies of anaesthesia in relation to hypertension. II. Haemodynamic consequences of induction and endotracheal intubation. Br J Anaesth 1971;43:531-47.
  9. REEMA GOEL, RAKA RANI, OP SING, DEEPAK MALAVIYA, S.K. ARYA: attenuation of cardiovascular response to laryngoscopy and intubation by various drugs in normotensive patients: Hospital today, 2000,9.
  10. REID LC, BRACE DE. Irritation of respiratory tract and its reflex effect upon heart. SurgGynec and Obstet. 1940; 70: 157-62.
  11. RUSSEL WJ, MORRIS RG, FREWN DB,DREW SE: ion changes in plasma catecholamine concentration during endotracheal intubation. Br J Anaesth, 1981 aug 53(8); 837-9.
  12. Seetharamaiah, S., Santhilatha, G.R., Rao, N., &VenugapalaRao, T. (2015). To evaluate the effect of intravenousdexmedetomidine (1 mcg/kg) as premedication in obtunding the pressor response to laryngoscopy and tracheal intubation compared to intravenous preservative-free 2% lignocaine (1.5-2 mg/kg). JournalofDental andMedicalSciences, 14(9), 37-43.
  13. STOELTING, ROBERT K. MD*. Blood Pressure and Heart Rate Changes During Short-Duration Laryngoscopy for Tracheal Intubation: Influence of Viscous or Intravenous Lidocaine. Anesthesia & Analgesia 57(2):p 197-199, March 1978.
Recommended Articles
Research Article Open Access
A Cross Sectional Study on Correlation Between Bispectral Index, End Tidal Sevoflurane Concentration, Difference in Inspiratory and End Tidal Oxygen Concentration for Anesthetic Depth Monitoring in Pediatric Patients Undergoing Short Surgeries
2025, Volume-6, Issue-5 : 483-487
Research Article Open Access
Prevalence And Foetal Outcomes of Thyroid Dysfunction and Anaemia in Pregnancy: A Retrospective Evaluation
2025, Volume-6, Issue-5 : 470-474
Research Article Open Access
Comparison Of Disease Severity and Outcome in Vaccinated and Non-Vaccinated COVID-19 Patients: A Prospective Observational Study
2025, Volume-6, Issue-5 : 461-469
Research Article Open Access
Effect of Gorlin's Sign as an active distraction technique on pain and behavioral response in pediatric patients during intravenous cannulation
2025, Volume-6, Issue-5 : 525-530
International Journal of Medical and Pharmaceutical Research journal thumbnail
Volume-6, Issue-5
Citations
1 Views
2 Downloads
Share this article
License
Copyright (c) International Journal of Medical and Pharmaceutical Research
Creative Commons Attribution License Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.
All papers should be submitted electronically. All submitted manuscripts must be original work that is not under submission at another journal or under consideration for publication in another form, such as a monograph or chapter of a book. Authors of submitted papers are obligated not to submit their paper for publication elsewhere until an editorial decision is rendered on their submission. Further, authors of accepted papers are prohibited from publishing the results in other publications that appear before the paper is published in the Journal unless they receive approval for doing so from the Editor-In-Chief.
IJMPR open access articles are licensed under a Creative Commons Attribution-ShareAlike 4.0 International License. This license lets the audience to give appropriate credit, provide a link to the license, and indicate if changes were made and if they remix, transform, or build upon the material, they must distribute contributions under the same license as the original.
Logo
International Journal of Medical and Pharmaceutical Research
About Us
The International Journal of Medical and Pharmaceutical Research (IJMPR) is an EMBASE (Elsevier)–indexed, open-access journal for high-quality medical, pharmaceutical, and clinical research.
Follow Us
facebook twitter linkedin mendeley research-gate
© Copyright IJMPR | All Rights Reserved