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Post Pancreatitis Complications Study (Based on a Prospective Data Base)

Withdrawn
Conditions
Pancreatitis
Interventions
Other: Collection of medical datas from ICU patients
Registration Number
NCT03284489
Lead Sponsor
Nantes University Hospital
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.

Detailed Description

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

Cross audit will be performed to check datas.

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • pancreatitis
Read More
Exclusion Criteria
  • consent withdrawal
Read More

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
ICU patientsCollection of medical datas from ICU patientsPatients with pancreatitis
Primary Outcome Measures
NameTimeMethod
In ICU stay main complicationsWithin 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
NameTimeMethod
Duration of Mechanical VentilationDuring ICU stay (up to 90 days)
Length of ICU stayDuring ICU stay (up to 90 days)

Trial Locations

Locations (5)

Poitiers University Hospital

🇫🇷

Poitiers, France

Rennes University Hospital

🇫🇷

Rennes, France

Tours University Hospital

🇫🇷

Tours, France

Angers University Hospital

🇫🇷

Angers, France

Nantes University Hospital

🇫🇷

Nantes, France

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