Actively Recruiting
Effect of Liberal Versus Restrictive Intravenous Fluid Administration on Postoperative Homeostasis in Patients Undergoing Laparoscopic Cholecystectomy
Led by King Edward Medical University · Updated on 2026-03-23
380
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating whether giving less intravenous (IV) fluid after surgery is as effective as giving more IV fluid in maintaining stable body functions among adults undergoing laparoscopic gallbladder removal (cholecystectomy). This study focuses on comparing restrictive versus liberal IV fluid administration to see how well both methods maintain vital signs such as blood pressure, heart rate, and urine output, as well as their impact on postoperative recovery and complications. Participants are randomly assigned to one of two groups after surgery: one group receives 1000ml of IV fluid (liberal administration) over 6 hours, and the other receives 500ml of IV fluid (restrictive administration) over the same period. These treatments are given perioperatively, meaning around the time of surgery, to evaluate differences in maintaining postoperative homeostasis. During the study, participants will have their vital signs—including pulse, blood pressure, and mean arterial pressure—monitored at multiple times after surgery: immediately, and at 3, 6, 12, and 24 hours. Urine output will also be recorded. The main outcome measured is mean systolic blood pressure on the first day after surgery, with additional monitoring of pulse rate, diastolic blood pressure, and pulse pressure. The total participation period covers the recovery phase following laparoscopic cholecystectomy.
CONDITIONS
Brief Title
Effect of Liberal and Restrictive IV Fluids on Recovery After Gallbladder Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- All patients undergoing elective cholecystectomy
- Age : 18-60 years
- All genders
- ASA class 1 and 2
You will not qualify if you...
- History of previous laparotomy
- Perforated gall bladder
- Duration of surgery more than 3 hours
- More than 100ml intra operative blood loss
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Perioperative period
Participants receive either 500ml or 1000ml of intravenous Lactated Ringer fluid during laparoscopic gallbladder surgery.
1 visit (in-person) on the day of surgery
Duration - 1 day
Participants are monitored after surgery for recovery and vital signs such as blood pressure and pulse rate.
1 follow-up visit (in-person) on Day 1 after surgery
Trial Site Locations
Total: 1 location
1
King Edward Medical University Lahore / Mayo Hospital Lahore
Lahore, Punjab Province, Pakistan, 54000
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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