- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06600828
Study's Care of Acute Pancreatitis at Saint-Etienne University Hospital.
Internal medicine units treat patients with undifferentiated or multisystem diseases, with a non-specific organ approach.
In some cases, patients with single-organ disease may be admitted to internal medicine wards. Acute pancreatitis is the most common gastrointestinal illness requiring acute admission to hospital. It is characterised by local and systemic inflammation of the pancreas corresponding to single-organ disease.
For patients with single-organ disease such as acute pancreatitis, it is not known whether admission to internal medicine is as effective as admission to a unit specialising in a specific organ, such as hepato-gastro-enterology.
Study Overview
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Kyria REGALADE, resident
- Phone Number: +33 (0)782651553
- Email: regaladekyria@gmail.com
Study Contact Backup
- Name: Baptiste GRAMONT, MD
- Phone Number: +33 (0)477829641
- Email: Baptiste.Gramont@chu-st-etienne.fr
Study Locations
-
-
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Saint-Etienne, France, 42055
- Recruiting
- CHU de Saint-Etienne
-
Contact:
- Kyria REGALADE, resident
- Phone Number: +33 (0)782651553
- Email: regaladekyria@gmail.com
-
Principal Investigator:
- Kyria REGALADE, resident
-
Sub-Investigator:
- Baptiste GRAMONT, MD
-
Sub-Investigator:
- Julie GOUTTE, MD
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- adult patient
- primary diagnosis of acute pancreatitis in Internal Medicine and gastroenterology.
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
The Internal Medicine Unit arm
It includes all patients hospitalized in the Internal Medicine Unit.
Patients may have been previously hospitalized in the emergency department or in another department such as intensive care.
|
Data collected: Socio-demographic, hospital, clinical, biological, and imaging data
|
|
The hepato-gastro-enterology Unit arm
It includes all patients hospitalized in the Gastroenterology unit.
Patients may have been previously hospitalized in the emergency department or in another department such as intensive care.
|
Data collected: Socio-demographic, hospital, clinical, biological, and imaging data
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Performance Stay Length Index
Time Frame: From the date of inclusion to the date of discharge from hospital, assessed for up to 100 months
|
"Performance Stay Length Index", is a measure used to evaluate the efficiency of hospital care in terms of patients' length of stay.
This index is calculated by comparing the average length of stay of patients in a given service to a predefined reference, often based on established standards or goals.
|
From the date of inclusion to the date of discharge from hospital, assessed for up to 100 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Rate of complications at 1 year
Time Frame: During one year from diagnosis
|
Number of complications documented in the computerized medical record, one year from diagnosis.
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During one year from diagnosis
|
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Rate of rehospitalization at 1 year
Time Frame: During one year from diagnosis
|
Number of hospitalizations documented in the computerized medical record, one year from diagnosis.
|
During one year from diagnosis
|
Collaborators and Investigators
Investigators
- Principal Investigator: Kyria REGALADE, resident, CHU Saint-Etienne
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRBN902024/CHUSTE
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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