Skip to main content
Clinical Trials/NCT06391762
NCT06391762
Completed
Not Applicable

Level of Deprivation Assessment in the Population of Short-bowel Syndrome With Intestinal Failure Patients Monitored by the Nancy University Hospital, France, Between 2020 and 2023

Central Hospital, Nancy, France1 site in 1 country92 target enrollmentDecember 28, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Short Bowel Syndrome
Sponsor
Central Hospital, Nancy, France
Enrollment
92
Locations
1
Primary Endpoint
Deprivation level
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The association between social deprivation and chronic disease is regularly examined but there are no data available on patients with intestinal failure due to short bowel syndrome (SBS-IF). First, the investigators aim to characterize this population and then to assess if insecurity is associated with some disease criteria.

Detailed Description

This exploratory cross-sectional study was conducted on patients affected by intestinal failure in short bowel syndrome and monitored by the certified home parenteral nutrition (HPN) center of Nancy University Hospital. The investigators included all patients over 18 years old suffering from SBS-IF followed-up by the certified HPN center of Nancy University Hospital between March 1st, 2020, and November 30th, 2023. The f-EDI (a European ecological index adapted to France) was determined for each participant. The investigators set the initial date at 2020, as this corresponds to the start of the use of patient-specific formulas in the center. Exclusion criteria were: not living in France, because it's required to use French-EDI and patients under 18 years old because they are monitored by the children's hospital. Investigators also excluded patients with transitory type 1 SBS who would have a bowel length over 2 meters after re-establishment of digestive continuity.

Registry
clinicaltrials.gov
Start Date
December 28, 2023
End Date
January 3, 2024
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Central Hospital, Nancy, France
Responsible Party
Principal Investigator
Principal Investigator

MICHOT Niasha

Principal Investigator

Central Hospital, Nancy, France

Eligibility Criteria

Inclusion Criteria

  • Patients over 18 years of age
  • Suffering from Short-bowel syndrome with intestinal failure
  • Monitored by the Certified Home Parenteral Nutrition Center of the Nancy University Hospital
  • Between March 1st 2020 and November 30th 2023

Exclusion Criteria

  • Patients not living in France
  • Transitory short-bowel syndrome with a predicted bowel length \> 200cm after digestive continuity

Outcomes

Primary Outcomes

Deprivation level

Time Frame: Throughout study completion, an average of 1 month

Determine the deprivation level of this population using the f-EDI of each participant

Secondary Outcomes

  • Association between deprivation level and disease characteristics(Throughout study completion, an average of 1 month)

Study Sites (1)

Loading locations...

Similar Trials