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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03284476
Other study ID # RC12_0207 doublon
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Status Withdrawn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 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.


Description:

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


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Status Withdrawn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:

- Nosocomial surgically treated Peritonitis

- Or Community-Acquired surgically treated Peritonitis

- Or Post-operative surgically treated Peritonitis

Exclusion Criteria:

- Consent withdrawal

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Collection of medical data from ICU patients
Medical data collected on a electronic secured data base

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 In ICU (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 first 28 days after ICU admission date
Secondary Duration of mechanical ventilation In ICU (up to 90 days)
Secondary ICU length of stay In ICU (up to 90 days)
See also
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Withdrawn NCT00463762 - Cefoperazone/Sulbactam In The Treatment Of Serious Intra-Abdominal And Hepatobiliary Infections. Phase 4
Active, not recruiting NCT02755610 - Check List to Improve Patient Self-care and Product Defect Report in Continuous Ambulatory Peritoneal Dialysis N/A
Not yet recruiting NCT05308849 - Peritoneal Diffusion and Efficacy of Antibiotic Therapy in Pediatric Peritonitis N/A
Completed NCT02726932 - Intra-abdominal View and Inflammatory Markers in Secondary Peritonitis - Correlation to Recovery
Recruiting NCT05050253 - Lavage With Super-Oxidized Solution for Secondary Peritonitis N/A
Completed NCT02926846 - IV Antibiotics With Lavage for Severe PD Peritonitis Phase 4