To compare two techniques of laparoscopic rectal prolapse surgery.
Phase 3
- Conditions
- Health Condition 1: K623- Rectal prolapse
- Registration Number
- CTRI/2020/12/030034
- Lead Sponsor
- Indira gandhi institute of medical sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1 All patients than 18-70 years presenting with full thickness rectal prolapse
2 medically cleared for general anesthesia
3 signed an informed consent.
Exclusion Criteria
1 Previous major abdominal surgery,
2.Slow transit constipation, Hirschsprungâ??s disease, inflammatory bowel disease, malignancy, diverticular disease and concomitant pelvic floor descent
3.Pregnancy,
4.Antidepressants or drugs that cause constipation, and
5.Patients with comorbid illnesses as severe cardiac disease or chronic renal failure
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome measures will be disappearance of prolapse and recurrences . <br/ ><br>Timepoint: 1 month <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1) Secondary outcomes- operating time (minutes) calculated from the first skin incision to the application of dressings; estimated blood loss (milliliters) recorded by the anesthesiologist; <br/ ><br> 2) conversion rate defined as unplanned laparotomy; <br/ ><br> 3) complications defined as alterations from the ideal postoperative course; <br/ ><br> 4) Hospital stay (days) defined as postoperative days. <br/ ><br> <br/ ><br>Timepoint: 7 days