Children Peritonitis Ecology at CHU de Rennes - (IIAPEDIA)

Sponsor
Rennes University Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT03668197
Collaborator
(none)
70
1
15.9
4.4

Study Details

Study Description

Brief Summary

The main objectif is assess the germs (species + antibiograms) implicated in children intra-abdominal infections (community acquired or nosocomial ) at CHU de Rennes.

Condition or Disease Intervention/Treatment Phase
  • Biological: microbiological analysis

Study Design

Study Type:
Observational
Anticipated Enrollment :
70 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Children Peritonitis Ecology at CHU de Rennes - (IIAPEDIA)
Actual Study Start Date :
Nov 23, 2017
Anticipated Primary Completion Date :
Jan 23, 2019
Anticipated Study Completion Date :
Mar 23, 2019

Outcome Measures

Primary Outcome Measures

  1. Blood Culture [2 weeks after inclusion]

    Ecology (germs resistance profile)

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Day to 18 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Children between 0 and 18 years old

  • Intra-abdominal infection with and indication for surgery or radiologically guided drainage.

  • No opposition from the child or his parents

Exclusion Criteria:
  • No microbiological sampling.

  • Primitive peritonitis (Spontaneous bacterial peritonitis, peritonitis during peritoneal dialysis)

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU de Rennes Rennes France 35033

Sponsors and Collaborators

  • Rennes University Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Rennes University Hospital
ClinicalTrials.gov Identifier:
NCT03668197
Other Study ID Numbers:
  • 35RC17_3086_IIAPEDIA
First Posted:
Sep 12, 2018
Last Update Posted:
Sep 12, 2018
Last Verified:
Sep 1, 2018
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 12, 2018