Haemorrhoidal Artery Ligation Study: the surplus value of the Doppler
Completed
- Conditions
- Haemorrhoids1001803110003184
- Registration Number
- NL-OMON30853
- Lead Sponsor
- Catharina-ziekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 92
Inclusion Criteria
Hemorrhoidal disease
Grade II or III
Symptomatic following two rubber-band-ligation-procedures
Written informed consent
Exclusion Criteria
Previous ano-rectal surgery
Known coagulation disorder
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>No more symptoms (blood loss, pain, pruritis, prolaps) at six months<br /><br>postoperatively</p><br>
- Secondary Outcome Measures
Name Time Method <p>Incidence of hamorrhages and bladder retentions first 48 hours<br /><br>Incidence of other repair related complications<br /><br>VAS pain score day 1-7<br /><br>VAS overall satisfaction month 1 + 6<br /><br>Wexner Fecal Incontinence Score month 1+6<br /><br>Costs<br /><br><br /><br>Maybe same questionairre one year postoperatively</p><br>