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Practice and effects of trans-anal bowel management systems

Practice and effects of trans-anal bowel management systems - PREFAB

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00021505
Enrollment
300
Registered
2020-06-03
Start date
2020-07-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

critical illness in general

Interventions

Group 1: Patients who receive a bowel management system for clinical and nursing indication

Sponsors

Universitätsmedizin Göttingen Klinik für Anästhesiologie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Patients in the intensive care units 0119 & 0116 of the UMG - Female, male and diverse patients - Age> 18 years - Supply with a transanal stool derivation system from a clinical nursing indication - Consent to participate in the study and answer the study-specific Questionnaire after discharge from the intensive care unit

Exclusion criteria

Exclusion criteria: - Age <18 years - no existing consent

Design outcomes

Primary

MeasureTime frame
Incontinence 3 months after discharge from the intensive care unit Stool incontinence questionnaire

Secondary

MeasureTime frame
Quality-of-live 3 months after discharge from the intensive care unit Questionnaire quality of life for stool incontinence

Countries

Germany

Contacts

Public ContactLars-Olav Harnisch

Universitätsmedizin Göttingen Klinik für Anästhesiologie

lars-olav.harnisch@med.uni-goettingen.de05513963579

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026