Overview

Effectiveness of Port Site Bupivacaine Injection in Postoperative Pain Reduction After Lap. Chole

Status:
Not yet recruiting
Trial end date:
2022-09-01
Target enrollment:
0
Participant gender:
All
Summary
To determine the effectiveness of port site bupivacaine infiltration in postoperative pain reduction after laparoscopic cholecystectomy.
Phase:
Phase 3
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Hamdard University
Treatments:
Bupivacaine
Criteria
Inclusion Criteria:

1. Patients of both the gender of age >18 years and <45years

2. Patients undergoing elective laparoscopic cholecystectomy under general anesthesia.

3. Patients with A.S.A grade I and II.

Exclusion Criteria:

1. Patients with known allergic reactions to local anesthetics.

2. Patients converted to open procedure.

3. Patients developing intra-operative complications.

4. Patients undergoing for laparoscopic cholecystectomy for acute cholecystitis.

5. Patients with obesity and chronic illness.

6. Patients with history of opioids, steroids, NSAIDs and alcohol use.