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Clinical Trials/ISRCTN32116071
ISRCTN32116071Active, not recruitingUnknown

Patient Reported Outcomes after parastomal hernia treatment - a prospective international cohort study

niversity of Birmingham0 sites1,500 target enrollmentStarted: August 17, 2023Last updated:

Trial Snapshot

Phase
Unknown
Status
Active, not recruiting
Enrollment
1,500

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Observational

Eligibility Criteria

Sex
All

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

Investigators

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