Skip to main content
Clinical Trials/NCT05214157
NCT05214157CompletedNot Applicable

A Prospective Randomized Controlled Study on the Role of Restoring Liver-Diaphragm Surface Tension and Pain Control at Port Sites in Optimizing Pain Management Following Laparoscopic Cholecystectomy

Zagazig University1 site in 1 country804 target enrollmentStarted: March 20, 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
804
Locations
1
Primary Endpoint
postoperative pain intensity

Study Overview

Brief Summary

evaluating the two final steps we added to optimize post laparoscopic cholecystectomy pain management.

Detailed Description

Introduction

After a laparoscopic cholecystectomy (LC), pain is still a significant concern, leading to extended hospital stays or readmissions. In majority of patients, postoperative pain medications are required. A standardized strategy is needed to offer effective pain relief postoperatively. The majority of pain in the early postoperative period is due to elimination of intraperitoneal surface tension or of parietal type. Aim of the work: to evaluate the two final steps we added to optimize postoperative pain management. Patients and methods: Over the period from March 2020 to December 2021, 816 patients with gallbladder stone undergoing LC were randomized into 2 groups after exclusion of 12 patients: Group A; interventional contained 402 patients. Group B; control contained 402 patients. Post-operative data to be compared were made in terms of operative time, shoulder pain, upper abdominal pain, (at 6,12,18 and 24 hours) and number of analgesic doses and hospital stay. Pain intensity was assessed by using the visual analogue scale (VAS) for each patient.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients who were having symptoms consistent with biliary colic,
  • had ultrasound evidence of gall stones,
  • classified as American Society of Anesthesiology (ASA) I and II
  • ages ranging from 18 to 65 years

Exclusion Criteria

  • Patients who refused to give consent,
  • pregnant,
  • had a history of drug abuse,
  • had CBD stones,
  • acute cholecystitis,
  • acute pancreatitis,
  • previous abdominal surgery,
  • history of peritonitis,
  • had carcinoma of the gall bladder Patients who were converted to open surgery,
  • patients who required placement of drains
  • patients with intraoperative complications (CBD injury or liver bed bleeding).

Outcomes

Primary Outcomes

postoperative pain intensity

Time Frame: 6 - 24 hours

severity by visual analogue scale

Secondary Outcomes

  • hospital stay(1-5 days)

Investigators

Sponsor Class
Other Gov
Responsible Party
Principal Investigator
Principal Investigator

Mohamed lotfy

Associate professor

Zagazig University

Study Sites (1)

Loading locations...

Similar Trials

Optimizing Pain Management Following... | Clinical Trial