Skip to content

Identifying the gene causing Congenital Short Bowel Syndrome

Identifying the gene causing Congenital Short Bowel Syndrome - Congenital Short Bowel Syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON35033
Enrollment
3
Registered
2010-05-27
Start date
2010-06-14
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

Congenital Short Bowel Syndrome

Interventions

None listed

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
2 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patient: Diagnosis of Congenital Short Bowel Syndrome Family member: Being a family member of a patient with Congenital Short Bowel Syndrome

Exclusion criteria

Exclusion criteria: Patient: Not a diagnosis of Congenital Short Bowel Syndrome Family member: not being a family member of a patient with Congenital Short Bowel Syndrome

Design outcomes

Primary

MeasureTime frame
Identification of the causative gene for CSBS

Secondary

MeasureTime frame
Geen

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)