The LaProS study. An international study to determine the optimal surgical treatment for rectal prolapse.
Recruiting
- Conditions
- Rectal prolapse (Full thickness, external)
- Registration Number
- NL-OMON25259
- Lead Sponsor
- Departmant of general surgery, Meander Medical Center, Amersfoort, The Netherlands.
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 240
Inclusion Criteria
All patients with an external rectal prolapse and an indication for laparoscopic ventral rectopexy (for European centers) or laparoscopic resection rectopexy (for US centers).
Exclusion Criteria
1. Under 18 years of age;
2. Former rectosigmoid resection;
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Improvement of Quality of life, objectified by the Gastro-intestinal Quality of life Index (GIQLI).
- Secondary Outcome Measures
Name Time Method