Clinical Trials Directory

Trials / Completed

CompletedNCT06964555

Effect of Intravenous Low-Dose Ketamine Infusion With Intravenous Lignocaine Infusion on Post-Operative Pain in Patients Undergoing Laparoscopic Choleysystectomy Under General Anesthesia

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Fazaia Ruth Pfau Medical College · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Objective: To determine the effect of low-dose ketamine versus lignocaine on post-operative pain in patients undergoing LC under general anesthesia in a tertiary care hospital. Sample Selection: Patients of both the gender of age at least 18 years, planned for elective LC with ASA grade I-II were included. Patients with obesity, history of alcohol consumptions, drug abusers, uncontrolled hypertension and diabetics, with chronic pain, allergic to study drugs, having neurological disorders, unable to understand pain scoring system and converted to open LC were excluded.

Conditions

Interventions

TypeNameDescription
DRUGIntravenous Ketamine InfusionsKetamine group received ketamine at 0.2mg/kg bolus intravenously followed by ketamine infusion at rate of 0.2mg/kg/hr throughout the surgery.
DRUGIntravenous lignocaineIV Lignocaine was given at the rate of 1 mg/kg/hr.

Timeline

Start date
2024-01-01
Primary completion
2024-11-30
Completion
2024-12-31
First posted
2025-05-09
Last updated
2025-05-22

Locations

1 site across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT06964555. Inclusion in this directory is not an endorsement.