- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00699933
Diagnostic and Interventional Therapy in Acute Pancreatitis
August 8, 2011 updated by: University of Regensburg
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.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
For laboratory values different inflammation markers were measured and compared.
Study Type
Observational
Enrollment (Anticipated)
50
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Tanja Bruennler, Dr. med.
- Phone Number: 7010 +49-941-944
- Email: tanja.bruennler@klinik.uni-r.de
Study Locations
-
-
-
Regensburg, Germany, 93053
- Recruiting
- Department of Internal medicine I, University of Regensburg
-
Contact:
- Tanja Bruennler, Dr. med.
- Phone Number: 7010 +43-941-944
- Email: tanja.bruennler@klinik.uni-r.de
-
Principal Investigator:
- Tanja Bruennler, Dr. med.
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
50 patients with acute pancreatitis
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
1
Evaluation of one study cohort
|
Evaluation of different diagnostics and evaluation of outcome of patients who received percutaneous CT-guided drainage for necrotic debridement and analyze the further outcome
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Length of hospital stay
Time Frame: weekly
|
weekly
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
time to surgery
Time Frame: weekly
|
weekly
|
active necrosectomy
Time Frame: weekly
|
weekly
|
ICU stay
Time Frame: weekly
|
weekly
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Jürgen Schölmerich, Prof., Director of Department of Internal Medicine I
- Study Director: Stefan Feuerbach, Prof., Director of Department of Radiology
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2008
Primary Completion (Anticipated)
December 1, 2012
Study Completion (Anticipated)
December 1, 2012
Study Registration Dates
First Submitted
June 13, 2008
First Submitted That Met QC Criteria
June 17, 2008
First Posted (Estimate)
June 18, 2008
Study Record Updates
Last Update Posted (Estimate)
August 9, 2011
Last Update Submitted That Met QC Criteria
August 8, 2011
Last Verified
June 1, 2010
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 08/008
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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