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Clinical Trials/NCT03284476
NCT03284476
Withdrawn
Not Applicable

A Prospective Cohort of Patients Hospitalized in West French Intensive Care Units for Peritonitis Surgically Treated

Nantes University Hospital5 sites in 1 countryApril 2013
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ConditionsPeritonitis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Peritonitis
Sponsor
Nantes University Hospital
Locations
5
Primary Endpoint
In ICU stay main complications
Status
Withdrawn
Last Updated
5 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The purpose of this observational study is to investigate the management and the complications associated wtih surgically treated peritonitis.

Data will be analysed to answer pre-defined scientific projects and to improve management of these conditions.

Detailed Description

Anonymous data will be collected by study coordinators in a secured e-database. Cross audit will be performed to check data.

Registry
clinicaltrials.gov
Start Date
April 2013
End Date
June 2020
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • •Nosocomial surgically treated Peritonitis
  • •Or Community-Acquired surgically treated Peritonitis
  • •Or Post-operative surgically treated Peritonitis

Exclusion Criteria

  • •Consent withdrawal

Outcomes

Primary Outcomes

In ICU stay main complications

Time Frame: Within the first 28 days after ICU admission date

Nosocomial Infections (epidemiology, risk factors, antibiotic susceptibility of pathogens) Organ failures (incidence, risk factors)

Secondary Outcomes

  • Duration of mechanical ventilation(In ICU (up to 90 days))
  • ICU length of stay(In ICU (up to 90 days))

Study Sites (5)

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