Trials / Unknown
UnknownNCT00793715
Laparotomy Versus Percutaneous Puncture in Patients With Abdominal Compartment Syndrome During Acute Pancreatitis
Decompressive Laparotomy With Temporary Abdominal Closure Versus Percutaneous Puncture With Placement of Abdominal Catheter in Patients With Abdominal Compartment Syndrome During Acute Pancreatitis:Multicenter, Randomised, Controlled Study
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 100 (estimated)
- Sponsor
- University of Belgrade · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
Decompressive laparotomy with temporary abdominal closure, will decrease of overall mortality and major morbidity in patients with abdominal compartment syndrome during acute pancreatitis in comparison with percutaneous puncture with placement of abdominal catheter.
Detailed description
We anticipated that decompressive laparotomy with temporary abdominal closure, beside all potentially negative side effects that early open surgery carries in patients with acute pancreatitis, results in decrease of overall mortality and major morbidity. The DECOMPRESS study is designed to compare effects of decompressive laparotomy with temporary abdominal closure and percutaneous puncture with placement of abdominal catheter in patients with abdominal compartment syndrome during acute pancreatitis.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Decompressive laparotomy with temporary abdominal closure | Surgical intervention including midline incision with temporary abdominal closure and several planed staged relaparotomies |
| PROCEDURE | Percutaneous puncture with placement of abdominal catheter | Installation of abdominal catheter percutaneously via abdominal centesis 2cm bellow the umbilicus |
Timeline
- Start date
- 2010-07-01
- Primary completion
- 2012-06-01
- Completion
- 2013-06-01
- First posted
- 2008-11-19
- Last updated
- 2010-07-26
Locations
5 sites across 1 country: Serbia
Source: ClinicalTrials.gov record NCT00793715. Inclusion in this directory is not an endorsement.