PROPHER: Quality-of-life feedback using patient-reported outcomes after treatment of parastomal hernia

Not Applicable

• Conditions: Parastomal hernia (PSH) treatment; Digestive System

• Registration Number: ISRCTN32116071
• Lead Sponsor: niversity of Birmingham

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-08-17
• Last Update Posted: 4 September 2023
• Study Completion: 2028-08-15

Recruitment & Eligibility

• Status: Ongoing
• Sex: All
• Target Recruitment: 1500

Inclusion Criteria

1. Adult, aged 18 years and above.
2. A stoma formed from any part of the bowel – whole small bowel and colon, and of any format – including loop, end, double barreled, Abcarian, other
3. All treatments for PSH, including conservative (non-operative) treatment and surgical intervention. All types of surgical approach are included.
4. Elective presentations to outpatient services, including surgical, colorectal, stoma care team are included. Patients presenting primarily as an emergency with a symptomatic PSH requiring urgent intervention are also eligible for inclusion, providing informed consent can be obtained.

Exclusion Criteria

1. Patients with an isolated urostomy
2. Life expectancy less than 12 months
3. Proposed treatment plan for dealing with PSH involves restoration of gut continuity meaning that patient will have no stoma after treatment.
4. Anyone who does not have an email address or does not have access to the internet or a smart device

Study & Design

• Study Type: Observational
• Study Design: Not specified