Post operative analgesia of Nefopam in laparoscopic surgery

Completed

• Conditions: Unspecified appendicitis,

• Registration Number: CTRI/2021/10/037110
• Lead Sponsor: Department of Anaesthesiology P D U medical college Rajkot

Brief Summary

This Study is a randomized , double blind ,parallel group single center trial comparing post operative analgesic effect of nefopam hydrochloride and diclofenac sodium in laparoscopic surgery . The primary outcome measures will be duration of post operative analgesia . The secondary outcome will be of effect of nefopam on post operative nausea and vomiting ,post operative shivering .

Detailed Description

Not available

Study Timeline

• Study Start: 2021-08-10
• Study Completion: 2021-11-15
• Last Update Posted: 2022-04-15

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

All Abdominal Laparoscopic surgeries of ASA grade 1 ,2, 3.

Exclusion Criteria

patient refusal, hepatic and renal insufficiency, patients on tricyclic anti depressants and MOA inhibitor , pregnancy and lactation , convulsive disorder.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Nefopam as compared to NSAIDS , due to its opioid sparing effect and no effect on platelet function it may prove to be useful non opioid adjuvant in laparoscopic abdominal surgeries	6-10 hours

Secondary Outcome Measures

Name	Time	Method
decreased post operative nausea and vomiting and post operative shivering	Baseline,1 hour , 2 hour

Trial Locations

Locations (1)

P D U MEDICAL COLLEGE RAJKOT; 🇮🇳 Rajkot, GUJARAT, India

P D U MEDICAL COLLEGE RAJKOT

🇮🇳Rajkot, GUJARAT, India

Darshan N

Principal investigator

7353543443

darshann59@gmail.com