Post Pancreatitis Complications Study (Based on a Prospective Data Base)
Sponsor
Nantes University Hospital (Other)
Overall Status
Withdrawn
CT.gov ID
NCT03284489
Collaborator
(none)
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5
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0
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Study Details
Study Description
Brief Summary
The purpose of this observational epidemiological study is to investigate the management and the complications associated with pancreatitis. Datas will be analysed to answer pre-defined scientific projects and to improve management of these conditions.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Detailed Description
Anonymous datas will be collected by study coordinators in a secured e-database.
Cross audit will be performed to check datas.
Study Design
Study Type:
Observational
Actual Enrollment
:
0 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Prospective Cohort of Patients With Pancreatitis Hospitalized in West French Intensive Care Units
Anticipated Study Start Date
:
Apr 1, 2013
Actual Primary Completion Date
:
Jun 1, 2020
Actual Study Completion Date
:
Jun 1, 2020
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| ICU patients Patients with pancreatitis |
Other: Collection of medical datas from ICU patients
Collection of medical datas from ICU patients with pancreatitis on a secured electronic database
|
Outcome Measures
Primary Outcome Measures
- In ICU stay main complications [Within the 28 first days after ICU admission date]
Nosocomial Infections (epidemiology, risk factors, antibiotic susceptibility of pathogens) Organ failures (incidence, risk factors)
Secondary Outcome Measures
- Duration of Mechanical Ventilation [During ICU stay (up to 90 days)]
- Length of ICU stay [During ICU stay (up to 90 days)]
Other Outcome Measures
- Death [During ICU stay (up to 90 days)]
Eligibility Criteria
Criteria
Ages Eligible for Study:
15 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
- pancreatitis
Exclusion Criteria:
- consent withdrawal
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Angers University Hospital | Angers | France | 49000 | |
| 2 | Nantes University Hospital | Nantes | France | 44093 | |
| 3 | Poitiers University Hospital | Poitiers | France | 86000 | |
| 4 | Rennes University Hospital | Rennes | France | 35000 | |
| 5 | Tours University Hospital | Tours | France | 37000 |
Sponsors and Collaborators
- Nantes University Hospital
Investigators
- Study Chair: Karim Asehnoune, MD,PhD, Non-Affiliated
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Nantes University Hospital
ClinicalTrials.gov Identifier:
NCT03284489
Other Study ID Numbers:
- RC12_0207 doublon 2
First Posted:
Sep 15, 2017
Last Update Posted:
Jun 4, 2020
Last Verified:
Jun 1, 2020
Keywords provided by Nantes University Hospital
Additional relevant MeSH terms: