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A clinical trial to study the effects of two drugs, intravenous paracetamol and intravenous tramadol for postoperative pain in patients undergoing laparoscopic cholecystectomy.

A comparative study to evaluate the clinical efficacy of Intravenous Paracetamol versus Intravenous Tramadol for postoperative pain in patients undergoing Laparoscopic Cholecystectomy. A Double Blind Randomized Control Trial. - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/077804
Enrollment
70
Registered
2024-12-06
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: K87- Disorders of gallbladder, biliarytract and pancreas in diseases classified elsewhere

Interventions

Intervention1: Administration of Intravenous Paracetamol for postoperative pain reduction.: To evaluate the clinical efficacy of 1g Intravenous Paracetamol for postoperative pain in patients undergoin

Sponsors

Heritage Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade I/II patients, Age between 18-60 years scheduled for elective laparoscopic cholecystectomy

Exclusion criteria

Exclusion criteria: Patients who had history of allergy to paracetamol or tramadol, Patients with severe pain (VAS = 5), Patients with signi ?cant coronary artery disease or ischemic myocardial disease, Patients with renal disease , liver disease , chronic lung disease and haemorrhagic conditions and/or coagulopathies, Patients with history of addiction to opioids or alcohol, Patient’s refusal

Design outcomes

Primary

MeasureTime frame
Intravenous paracetamol provides better management in postoperative pain in patients undergoing laparoscopic cholecystectomy. Timepoint: Pain score before drug administration (T0), 30th minute (T1), 2nd hour (T2), 4th hour (T3), 8th hour (T4), 16th hour (T5), 24th hour (T6). Haemodynamic parameters at 0 minute, 30 minutes, 2 hr, 4 hr, 8 hr, 16 hr, 24 hr.

Secondary

MeasureTime frame
Intravenous paracetamol has lesser side effects as compared to intravenous tramadol. Timepoint: Haemodynamic parameters at 0 minute, 30 minutes, 2 hr, 4 hr, 8 hr, 16 hr, 24 hr. Prevalence of Adverse effects – Nausea, Vomiting, Dizziness, Drowsiness

Countries

India

Contacts

Public ContactAkhilesh Mishra

Heritage Institute of Medical Sciences

akhil61086@rediffmail.com9582113920

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026