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WithdrawnNCT03284489Updated Jun 4, 2020

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

An observational study in Pancreatitis, sponsored by Nantes University Hospital. Withdrawn at 5 sites in France. Open to participants aged 15 Years and older. Per ClinicalTrials.gov, last updated 2020-06-04.

Sponsored by Nantes University Hospital · Observational

Why this study was withdrawn
No inclusion
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
0
Ages
15 Years and older
Sex
All
01

Study 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.

Read the detailed description

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

Cross audit will be performed to check datas.

02

Conditions studied

  • Pancreatitis

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Keywords

  • Pancreatitis
03

Who can participate

Ages eligible
15 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with pancreatitis hospitalized in ICU

Inclusion criteria

  • pancreatitis

Exclusion criteria

Exclusion Criteria:

  • consent withdrawal
04

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
0 participants (actual)
Patient registry
No

Groups and cohorts

  • ICU patients

    Patients with pancreatitis

    Other: Collection of medical datas from ICU patients

Interventions

  • OtherCollection of medical datas from ICU patients

    Collection of medical datas from ICU patients with pancreatitis on a secured electronic database

05

What researchers measure

Primary outcomes

  1. In ICU stay main complications

    Nosocomial Infections (epidemiology, risk factors, antibiotic susceptibility of pathogens) Organ failures (incidence, risk factors)

    Time frame: Within the 28 first days after ICU admission date

Secondary outcomes

  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 outcomes

  1. Death

    Time frame: During ICU stay (up to 90 days)

06

Study locations

5 sites
  • Angers University Hospital
    Angers, 49000, France
  • Nantes University Hospital
    Nantes, 44093, France
  • Poitiers University Hospital
    Poitiers, 86000, France
  • Rennes University Hospital
    Rennes, 35000, France
  • Tours University Hospital
    Tours, 37000, France
07

Registry details

Key details

Study ID
NCT03284489
Lead sponsor
Nantes University Hospital
Responsible party
Sponsor
First posted
Sep 15, 2017
Start date
Apr 2013 (estimated)
Primary completion
Jun 2020
Completion
Jun 2020
Last update
Jun 4, 2020

Study contacts

Karim Asehnoune, MD,PhD
study chair · Non-Affiliated

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Jun 2020. You cannot join it, but the record below documents what was studied.

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