Comparision of nerve block with opiod in relieving pain of patients with acute pancreatitis
Phase 2
- Conditions
- Health Condition 1: K859- Acute pancreatitis, unspecifiedHealth Condition 2: 3- Administration
- Registration Number
- CTRI/2024/01/061167
- Lead Sponsor
- Department of Emergency Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Adults patients (= 18 years of age) who are
already diagnosed as acute or recurrent
acute pancreatitis, presenting to the
emergency department of AIIMS New
Delhi within 7 days of onset of abdominal
pain with DVPRS = 7.
2. Patients willing to give consent.
Exclusion Criteria
1. Patients with hemodynamic instability
2. Patients having one or more organ
dysfunction
3. Patients allergic to drugs
4. Local site infection
5. Spine deformity (both acquired or
congenital)
6. Pregnancy
7. Immunosuppressive state
8. Patients with chronic kidney disease,
chronic liver disease, congestive heart
failure
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the efficacy of successful pain relief (more than 50% reduction in pain score by Defense and Veterans Pain Scale(DVPRS) from presentation or DVPRS less than 4 or total <br/ ><br>amount of rescue analgesia needed) after six hours of intervention in both ESPB arm <br/ ><br>and conventional pharmacological therapy (CPT) arm.Timepoint: Primary outcome will be assessed and analysed after six hours of intervention in both ESPB arm <br/ ><br>and conventional pharmacological therapy (CPT) arm.
- Secondary Outcome Measures
Name Time Method