Skip to content

TO COMPARE THE EFFICACY OF TWO ANALGESICS:DICLOFENAC AND TRAMADOL IN RELIEVING PAIN IN PATIENTS OF ACUTE PANCREATITIS â?? A PILOT STUDY

TO COMPARE THE EFFICACY OF DICLOFENAC AND TRAMADOL IN RELIEVING PAIN IN PATIENTS OF ACUTE PANCREATITIS â?? A PILOT STUDY

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/05/014309
Enrollment
45
Registered
2018-05-31
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Pain in Acute pancreatitis

Interventions

Intervention1: Intravenous diclofenac: Intravenous diclofenac 1 mg/kg was administered in adult patients with acute pancreatitis presenting within 3 days of onset of pain as a 2nd comparator arm of t

Sponsors

PGIMER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Informed consent. 2. Patients more than 18 years of age. 3.Acute pancreatitis as defined by clinical symptoms, elevated serum amylase (more than thrice the upper limit of normal range) or imaging findings. 4. Patients who have presented to the hospital within the first 3 days after onset of pain. 5. Alert and oriented at admission.

Exclusion criteria

Exclusion criteria: 1. Pregnancy 2. Patients with significant chronic hepatitis, anaemia and agranulocytosis. 3.Patients of acute pancreatitis who have renal failure (Serum Creatinine >= 1.4 mg/dl) at presentation 4.Patients who were contraindicated to Opioids and NSAIDS 5. Patients Who already are taking or have taken opioids and NSAIDS for other reasons ï??No written informed consent ï??Deaths during study

Design outcomes

Primary

MeasureTime frame
1.Number of participants showing improvement in pain intensity. 2.Number of participants requiring supplementary analgesia (offered when trial drug intervention fails to relieve pain). Timepoint: Pain scores were recorded after first hour (VAS1) of administration of the drug and subsequently every 3 hours by a blinded researcher using the VAS for assessing pain intensity. The study medication was limited to maximum period of seven days and stopped earlier if there was no further need for analgesia. A painless day was defined as being a day when a patient mark zero on VAS.

Secondary

MeasureTime frame
1.Number of participants with pancreatitis complications. 2.Number of participants with drug related adverse events. 3.To determine correlation between lipase concentration on admission and dose of analgesia requirement. 4.Number of deaths from any cause. Timepoint: No time point

Countries

India

Contacts

Public ContactDr Santosh Kumar Nadipalli

PGIMER chandigarh

dr_kochhar@hotmail.com

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 20, 2026