Assessing clinical effects and patient perspectives of a tailored parastomal ‘Hernia Halt’ in managing patient symptoms of parastomal hernias

Not Applicable

• Conditions: Parastomal hernia; Oral and Gastrointestinal - Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon

• Registration Number: ACTRN12623001175662
• Lead Sponsor: niversity of Otago

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-11-14
• Last Update Posted: 20 November 2023

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 15

Inclusion Criteria

1)Patients who have a parastomal hernia
2) Patients currently residing in the Te Whatu Ora Southern catchment

Exclusion Criteria

1)Inability to provide consent
2)Inability to converse in English
3)Patients who have an asymptomatic parastomal hernia

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Quality of life[Patient reported quality of life using the SF-36 quality of life questionnaire (Ware, John E., K. K. Snow, M. Kosinski, and B. Gandek. The SF-36 health survey. Manual and interpretation guide 2 (1996).) At baseline prior to wearing the guard and after four weeks of wearing the guard];Pain[100 mm visual analogue pain scale anchored with none and worst imaginable At baseline prior to wearing the guard and after four weeks of wearing the guard]