Single Dose vs Double dose of low molecular weight heparin in treatment of Severe Acute Pancreatitis
Phase 3
- Conditions
- Health Condition 1: K859- Acute pancreatitis, unspecified
- Registration Number
- CTRI/2021/01/030610
- Lead Sponsor
- ILBS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All adult cases of severe acute pancreatitis , who do not match exclusion criteria ,admitted to ILBS during study period will be included in the study .
Exclusion Criteria
Patients with:
-chronic pancreatitis.
-hypersensitivity to LMWH
-Pregnant or breast feeding ladies
- pediatric age group
- prior coagulopathy.
- CLD with acute pancreatitis.
- Stroke/ CVA(Cerebro-Vascular Accident)
- Established SP axis thrombus
- Presentation beyond 10 days from onset of pancreatitis
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Objective comparison of clinical degree of severity and organ failure scores in the two arms as evaluated by SOFA, APACHE II scores at day 7 and day 14 of therapyTimepoint: Baseline, Day 7 and Day 14 of therapy.
- Secondary Outcome Measures
Name Time Method 1.In hospital mortality. <br/ ><br>2.Duration of ICU Stay <br/ ><br>3.Duration of Hospital stay <br/ ><br> 4. Thrombotic complications- SPM-axis thrombosis <br/ ><br> 5.Haemorrhagic complications- GI haemorrhage, Intra-pancreatic haemorrhage, Post intervention haemorrhage. <br/ ><br>6.Need for IR, MIS, Surgery for local complications. <br/ ><br>7.Coagulopathy: Changes in ROTEM <br/ ><br>8.CRP level at day 3, 7, 14 <br/ ><br>Timepoint: At admission, day 3, day 7, day 14 and throughout hospital stay depending upon parameter as mentioned in secondary outcome parameteres.