Post Surgically Treated Peritonitis Complications

Withdrawn

• Conditions: Peritonitis
• Interventions: Other: Collection of medical data from ICU patients

• Registration Number: NCT03284476
• Lead Sponsor: Nantes University Hospital

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.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2013-04
• Study First Submitted: 2017-09-14
• Study First Submitted QC: 2017-09-14
• Study First Posted: 2017-09-15
• Status Verified: 2020-06
• Primary Completion: 2020-06
• Study Completion: 2020-06
• Last Update Submitted: 2020-06-02
• Last Update Posted: 2020-06-04

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

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

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Exclusion Criteria

• Consent withdrawal

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
ICU patients	Collection of medical data from ICU patients	Collection of medical data of Patients with peritonitis (nosocomial or community-acquired) or Patients with post-operative peritonitis

Primary Outcome Measures

Name	Time	Method
In ICU stay main complications	Within the first 28 days after ICU admission date	Nosocomial Infections (epidemiology, risk factors, antibiotic susceptibility of pathogens) Organ failures (incidence, risk factors)

Secondary Outcome Measures

Name	Time	Method
Duration of mechanical ventilation	In ICU (up to 90 days)
ICU length of stay	In ICU (up to 90 days)

Trial Locations

Locations (5)

Poitiers University Hospital; 🇫🇷 Poitiers, France

Angers University Hospital; 🇫🇷 Angers, France

Nantes University Hospital; 🇫🇷 Nantes, France

Rennes University Hospital; 🇫🇷 Rennes, France

Tours University Hospital; 🇫🇷 Tours, France