assess the post-operative complications and functional outcome among patients planned to undergo TURP
Phase 3
- Conditions
- Health Condition 1: N401- Benign prostatic hyperplasia withlower urinary tract symptomsHealth Condition 2: N401- Benign prostatic hyperplasia withlower urinary tract symptoms
- Registration Number
- CTRI/2024/02/062292
- Lead Sponsor
- on sponsored
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patients above 40 years of age.
2. Patients who will be willing to give consent and time of data collection in the study.
3. Patients who can understand Hindi or English.
Exclusion Criteria
1. Patients, who will not be able to receive, understand or respond to instructions.
2. Patients who had an open prostatectomy, A patient who had unsuccessful TURP.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Functional outcome that will be assessed by IIEF and IPSSTimepoint: IPSS in 1 month and IIEF in 3 months
- Secondary Outcome Measures
Name Time Method Post-operative complicationsTimepoint: 1 month