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Level of Deprivation Assessment in a Population of Short-bowel Syndrome Patients With Intestinal Failure

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06391762
Acronym
PRECAR-SGC
Enrollment
92
Registered
2024-04-30
Start date
2023-12-28
Completion date
2024-01-03
Last updated
2024-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Deprivation, Psychosocial, Intestinal Failure, Short Bowel Syndrome

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.

Interventions

None listed

Sponsors

Central Hospital, Nancy, France
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

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

Design outcomes

Primary

MeasureTime frameDescription
Deprivation levelThroughout study completion, an average of 1 monthDetermine the deprivation level of this population using the f-EDI of each participant

Secondary

MeasureTime frameDescription
Association between deprivation level and disease characteristicsThroughout study completion, an average of 1 monthDetermine the association between the deprivation level of the patients with SBS-IF determined by f-EDI and the characteristics of their disease

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026