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Comparing Tramadol vs Paracetamol for Pain Relief in Acute Pancreatitis: A Randomized Controlled Trial

To Compare the Efficacy and Safety of Intravenous Tramadol versus Intravenous Paracetamol as Analgesics in Patients of Acute Pancreatitis: A Prospective, Randomized Control Trial - nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068751
Enrollment
80
Registered
2024-06-12
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: K859- Acute pancreatitis, unspecified

Interventions

Intervention1: paracetamol: paracetamol I.V 1000mg/100ml Normal Saline three times a day for 7 days Control Intervention1: tramadol: tramadol I.V 50mg/100 ml Normal Saline three times a day for 7day

Sponsors

DR ABHIJEET SHRIDHAR
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of age 18 or more, with diagnosis of Acute Pancreatitis, Irrespective of severity 2. Acute pancreatitis will be diagnosed according to revised Atlanta Classification 2012, which require 2 or more of the following criteria be met for the diagnosis; (a) Abdominal pain suggestive of pancreatitis (b) Serum amylase or lipase level greater than three times the upper normal value (c) Characteristic imaging findings

Exclusion criteria

Exclusion criteria: 1. Patients with severe hepatic impairment & severe renal impairment (Creatinine clearance less than 30mL/min) 2. Ongoing treatments with NSAIDs (within 24hrs) 3. History of allergy to paracetamol and/or tramadol

Design outcomes

Primary

MeasureTime frame
1.To Determine the effectiveness of Intravenous Paracetamol and Intravenous Tramadol in treating pain. 2. To Compare. pain alleviation between Paracetamol and Tramadol 3. Analyzing patient-reported pain intensity outcomes 4. Potentially assessing adverse events or adverse drug reactions with Paracetamol and Tramadol Timepoint: 18-24 months

Secondary

MeasureTime frame
1. The duration of pain alleviation provided by Tramadol & Paracetamol 2. Assessing the impact of these medications on hospital stays or re-admission rates 3. Examining overall patient satisfaction with pain management Timepoint: 18-24 months

Countries

India

Contacts

Public ContactDR JAMEEL AHMAD

Jawaharlal Nehru Medical College and Hospital, Aligarh Muslim University

ahmad.drjameel@gmail.com7599529550

Outcome results

None listed

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