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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03284489
Other study ID # RC12_0207 doublon 2
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date April 2013
Est. completion date June 2020

Study information

Verified date June 2020
Source Nantes University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Description:

Anonymous datas will be collected by study coordinators in a secured e-database.

Cross audit will be performed to check datas.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date June 2020
Est. primary completion date June 2020
Accepts healthy volunteers No
Gender All
Age group 15 Years and older
Eligibility Inclusion Criteria:

- pancreatitis

Exclusion Criteria:

- consent withdrawal

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Collection of medical datas from ICU patients
Collection of medical datas from ICU patients with pancreatitis on a secured electronic database

Locations

Country Name City State
France Angers University Hospital Angers
France Nantes University Hospital Nantes
France Poitiers University Hospital Poitiers
France Rennes University Hospital Rennes
France Tours University Hospital Tours

Sponsors (1)

Lead Sponsor Collaborator
Nantes University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Other Death During ICU stay (up to 90 days)
Primary In ICU stay main complications Nosocomial Infections (epidemiology, risk factors, antibiotic susceptibility of pathogens) Organ failures (incidence, risk factors) Within the 28 first days after ICU admission date
Secondary Duration of Mechanical Ventilation During ICU stay (up to 90 days)
Secondary Length of ICU stay During ICU stay (up to 90 days)
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