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Multicentre Observational Study on Community Acquired Intraabdominal Infections Management (PERICOM)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03544203
Recruitment Status : Completed
First Posted : June 1, 2018
Last Update Posted : May 3, 2019
Sponsor:
Information provided by (Responsible Party):
Centre Hospitalier Universitaire de Nīmes

Brief Summary:
Intraabdominal infection require rapid care management including antibiotic therapy and source control. Morbidity and mortality associated with Intraabdominal infections remain high. French recommendations have been edited in 2000 further updated in 2014. Delay in diagnosis and surgery can lead to worsened outcomes. However, little data are available on early community-acquired intraabdominal infections management to identify risk factors of inadequate management.

Condition or disease
Intraabdominal Infections

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Study Type : Observational
Actual Enrollment : 200 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Multicentre Observational Study on Community Acquired Intraabdominal Infections Management: the PERICOM Study
Actual Study Start Date : April 1, 2018
Actual Primary Completion Date : February 28, 2019
Actual Study Completion Date : March 30, 2019



Primary Outcome Measures :
  1. length of stay [ Time Frame: 6 month ]


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
patients admitted to emergency department for a diagnosis of proven or suspected intraabdominal infection requiring surgery
Criteria

Inclusion Criteria:

  • ≥ 18 years
  • patients admitted to emergency department for a diagnosis of proven or suspected intraabdominal infection requiring surgery

Exclusion Criteria:

  • primary intraabdominal infection
  • health-care associated intraabdominal infection
  • abdominal trauma
  • patient under guardianship
  • opt out consent
  • patient already enrolled in the present study

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03544203


Locations
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France
CHU d'Amiens
Amiens, France, 80054
CHU Angers
Angers, France, 49033
Hia Percy
Clamart, France
CHU Clermont-Ferrand
Clermont-Ferrand, France, 63000
Hôpital Henri Mondor
Créteil, France, 94010
CHU Grenoble La Tronche
Grenoble, France, 38700
CHRU Lille
Lille, France, 59037
Lyon-Sud Pierre Bénite
Lyon, France
AP HM La Timone
Marseille, France, 13385
Ap Hm La Timone
Marseille, France
CHU Nimes
Nîmes, France, 30029
CHU Bichat Claude Bernard
Paris, France, 75018
Le Kremlin-Bicêtre
Paris, France, 94270
CHU Strasbourg
Strasbourg, France
Sponsors and Collaborators
Centre Hospitalier Universitaire de Nīmes
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Responsible Party: Centre Hospitalier Universitaire de Nīmes
ClinicalTrials.gov Identifier: NCT03544203    
Other Study ID Numbers: 2017-A03407-46
First Posted: June 1, 2018    Key Record Dates
Last Update Posted: May 3, 2019
Last Verified: January 2019

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Centre Hospitalier Universitaire de Nīmes:
intraabdominal infections
peritonitis
critically ill
Additional relevant MeSH terms:
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Infection
Communicable Diseases
Intraabdominal Infections