se of platelet rich plasma(PRP) as an adjunct in the treatment of high peri-anal fistulas.
Recruiting
- Conditions
- fistula1000211210017998
- Registration Number
- NL-OMON43622
- Lead Sponsor
- Medisch Universitair Ziekenhuis Maastricht
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 120
Inclusion Criteria
no bias to sex, age 16-80 years, able to understand informed consent, high peri-anal fistula
Exclusion Criteria
-inability to fullfill follow-up criteria
-pregnant
-local malignancy
-Crohn*s disease/Ulcerative colitis
-patients with a traumatic/iatrogenic lesion
-Trombocytopenia
- Splenomegaly
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Main study parameters/endpoint primary: recurrence rate</p><br>
- Secondary Outcome Measures
Name Time Method <p>Main study parameters/endpoints secundary: post-operative pain, continence,<br /><br>quality of life.</p><br>