A clinical trial to study the safety and practicability of mono polar urethral route removal of prostate without post-surgery urinary catheter traction in patients with enlarged prostate
Not Applicable
- Conditions
- Health Condition 1: N998- Other intraoperative and postprocedural complications and disorders of genitourinary system
- Registration Number
- CTRI/2022/01/039199
- Lead Sponsor
- Abhineeth K P
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
prostate size of 30-80 ml
Exclusion Criteria
1) Patients refusing to participate/give consent.
2) Patients failed to achieve Intraoperative
hemostasis.
3) Patients with both BPH and bladder tumor
4) Patients with both BPH and bladder stone
5) Patients with both BPH and Urethral stricture
disease
6) Patients with both BPH and meatal stenosis
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1) To compare pain scores <br/ ><br>2) to compare the post operative blood lossTimepoint: 1) pain scores - using visual analogue score will be recorded at 6 hour,12 hour and 18 hour post surgery <br/ ><br>2) Blood loss will be calculated using Bourkeâ??s formula , preopertaive hematocrit and postoperative hematocrit will be evaluated at post operative day one.
- Secondary Outcome Measures
Name Time Method 1.To compare the duration of hospital stay. <br/ ><br>2.To compare the incidence of bladder washouts and clot retention. <br/ ><br>3.To compare the incidence of deep venous thrombosis <br/ ><br>Timepoint: 1)Duration of hospital stay. (Calculated from the day of surgery to day of discharge) <br/ ><br>2)The incidence of bladder washouts and clot retention <br/ ><br>3)The incidence of deep vein thrombosis <br/ ><br>