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Post Pancreatitis Complications Study (Based on a Prospective Data Base)

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ClinicalTrials.gov Identifier: NCT03284489
Recruitment Status : Active, not recruiting
First Posted : September 15, 2017
Last Update Posted : September 28, 2017
Sponsor:
Information provided by (Responsible Party):
Nantes University Hospital

Brief Summary:
The purpose of this observational epidemiological study is to investigate the management and the complications associated with pancreatitis. Datas will be analysed to answer pre-defined scientific projects and to improve management of these conditions.

Condition or disease Intervention/treatment
Pancreatitis Other: Collection of medical datas from ICU patients

Detailed Description:

Anonymous datas will be collected by study coordinators in a secured e-database.

Cross audit will be performed to check datas.


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Study Type : Observational
Estimated Enrollment : 300 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Prospective Cohort of Patients With Pancreatitis Hospitalized in West French Intensive Care Units
Study Start Date : April 2013
Estimated Primary Completion Date : December 2050
Estimated Study Completion Date : December 2050

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Pancreatitis

Group/Cohort Intervention/treatment
ICU patients
Patients with pancreatitis
Other: Collection of medical datas from ICU patients
Collection of medical datas from ICU patients with pancreatitis on a secured electronic database




Primary Outcome Measures :
  1. In ICU stay main complications [ Time Frame: Within the 28 first days after ICU admission date ]
    Nosocomial Infections (epidemiology, risk factors, antibiotic susceptibility of pathogens) Organ failures (incidence, risk factors)


Secondary Outcome Measures :
  1. Duration of Mechanical Ventilation [ Time Frame: During ICU stay (up to 90 days) ]
  2. Length of ICU stay [ Time Frame: During ICU stay (up to 90 days) ]

Other Outcome Measures:
  1. Death [ Time Frame: During ICU stay (up to 90 days) ]


Information from the National Library of Medicine

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Ages Eligible for Study:   15 Years and older   (Child, Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients with pancreatitis hospitalized in ICU
Criteria

Inclusion Criteria:

  • pancreatitis

Exclusion Criteria:

  • consent withdrawal

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): NCT03284489


Locations
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France
Angers University Hospital
Angers, France, 49000
Nantes University Hospital
Nantes, France, 44093
Poitiers University Hospital
Poitiers, France, 86000
Rennes University Hospital
Rennes, France, 35000
Tours University Hospital
Tours, France, 37000
Sponsors and Collaborators
Nantes University Hospital
Investigators
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Study Chair: Karim Asehnoune, MD,PhD Non-Affiliated

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Responsible Party: Nantes University Hospital
ClinicalTrials.gov Identifier: NCT03284489     History of Changes
Other Study ID Numbers: RC12_0207 doublon 2
First Posted: September 15, 2017    Key Record Dates
Last Update Posted: September 28, 2017
Last Verified: September 2017
Keywords provided by Nantes University Hospital:
Pancreatitis
Additional relevant MeSH terms:
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Pancreatitis
Pancreatic Diseases
Digestive System Diseases