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A clinical trial to study effects of two drugs,ibuprofen and paracetamol in patients undergoing laparoscopic cholecystectomy surgery

Efficacy of Intravenous Ibuprofen and Paracetamol on Postoperative Pain and Tramadol Consumption After Laparoscopic Cholecystectomy Surgery: A Prospective, Randomized, Clinical Trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/088605
Enrollment
80
Registered
2025-06-11
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K811- Chronic cholecystitis Health Condition 2: K804- Calculus of bile duct with cholecystitis Health Condition 3: 3- Administration

Interventions

Intervention1: Intravenous Ibuprofen: Intravenous Ibuprofen Dosage: 800 mg Route: Intravenous infusion Timing: Administered 30 minutes before the end of laparoscopic cholecystectomy Frequency: Sin

Sponsors

Lakshman P
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients Aged 18 To 85 Years. Patients With American Society of Anesthesiologists (ASA) Physical Status Scores Ranging From 1 To 3. Patients Who Are Given Consent and Willing to Participate in This Study.

Exclusion criteria

Exclusion criteria: Patients Classified as Having an ASA Score of IV Those Falling Outside the Specified Age Range. Individuals With Peptic Ulcers, Severe Hepatic or Renal Failure, Significant Cardiovascular or Pulmonary Conditions. A History of Drug Allergies (Specifically, Propofol, Fentanyl, Rocuronium, Paracetamol, Ibuprofen, And Tramadol). As Well As Cases of Emergency Surgery. Individuals Who Did Not Provide Informed Consent.

Design outcomes

Primary

MeasureTime frame
The primary objective of this study was to assess and compare the impact of iv ibuprofen and paracetamol on postoperative pain intensity through numeric rating scale .Timepoint: Post operative 1st, 6th, 12th, and 24th hours

Secondary

MeasureTime frame
As secondary objectives, this study assesses tramadol consumption as rescue analgesic, analyzes intraoperative hemodynamic parameters, and the investigates any adverse effects related to study drugs in patients who underwent laparoscopic cholecystectomy surgery.Timepoint: intraoperatively baseline , 5minutes ,10minutes ,30minutes ,60minutes ,90minutes ,120minutes postoperatively 1st hour ,6th hour ,12th hour ,24th hour

Countries

India

Contacts

Public ContactDr Rajeev Kumar Dubey

Institute of Medical Sciences BHU

rajeevdubeyrk@gmail.com9839927283

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026