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NCT00699933 Clinical Trial

Diagnostic and Interventional Therapy in Acute Pancreatitis

Acute Pancreatitis Clinical Trial

Official title:
Diagnostic and Interventional Therapy in Acute Pancreatitis

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00699933
Other study ID # 08/008
Secondary ID
Status Recruiting
Phase N/A
First received June 13, 2008
Last updated August 8, 2011
Start date May 2008
Est. completion date December 2012

Study information
Verified date June 2010
Source University of Regensburg
Contact Tanja Bruennler, Dr. med.
Phone +49-941-944
Email tanja.bruennler@klinik.uni-r.de
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Observational

Clinical Trial Summary

The study aims to evaluate the course of patients with acute pancreatitis. Thereby we analyze different diagnostics and compare ultrasound, MRI and CT-scan in detection of necrotic areas and evaluate interventional therapy methods like percutaneous drainage techniques regarding the outcome. Laboratory values were assessed as well.

Description:

For laboratory values different inflammation markers were measured and compared.

Recruitment information / eligibility
Status Recruiting
Enrollment 50
Est. completion date December 2012
Est. primary completion date December 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age > 18 years

- Acute pancreatitis

- Written formal consent

Exclusion Criteria:

- Pregnancy

- Missing formal consent

- Individual contraindications for CT-scan

- MRI or endoscopic ultrasound

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Other:
• CT-guided percutaneous drainage technique
Evaluation of different diagnostics and evaluation of outcome of patients who received percutaneous CT-guided drainage for necrotic debridement and analyze the further outcome

Locations
Country Name City State
Germany Department of Internal medicine I, University of Regensburg Regensburg

Sponsors (1)
Lead Sponsor Collaborator
University of Regensburg

Country where clinical trial is conducted

Germany, 

Outcome
Type Measure Description Time frame Safety issue
Primary Length of hospital stay weekly No
Secondary time to surgery weekly No
Secondary active necrosectomy weekly No
Secondary ICU stay weekly No
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