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Comparison of effectiveness of Dexmedetomidine in low dose to provide pain relief, when administered either Intravenously or inside abdomen during laparoscopic Cholecystectomy

Phase 4
Completed
Conditions
Health Condition 1: null- Patients undergoing laparoscopic cholecystectomy for Gall stone disease
Registration Number
CTRI/2017/11/010456
Lead Sponsor
niversity College of Medical Sciences and GTB Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. ASA I and II patients

2. Aged 18-50 years,

3. Undergoing laparoscopic cholecystectomy under GA

Exclusion Criteria

1. BMI > 30 kg/m2

2. Allergy to any medication

3. Renal or hepatic insufficiency

4. Neurologic and psychiatric disease

4. Preoperative HR < 45/min

5. On antihypertensive medication with any α2 adrenergic agonists e.g. clonidine

6.surgical procedure converted to open cholecystectomy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Time to the first request of analgesia in the postâ??operative periodTimepoint: 24 hours postâ??operative period
Secondary Outcome Measures
NameTimeMethod
1. Total dose of diclofenac consumption in 24 h period (postâ??operative) <br/ ><br>2. Visual analogue scale [VAS]) pain score <br/ ><br>3. Any adverse/side effects. <br/ ><br>Timepoint: 24 h period postâ??operative
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