A randomized study about TURP complications due to Asiprin consumptio
Not Applicable
- Conditions
- Trasurethral resection of prostat.
- Registration Number
- IRCT20200122046220N1
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Male
- Target Recruitment
- 132
Inclusion Criteria
Benign Prostatic Hyperplasia
Exclusion Criteria
End Stage Renal Disease (ESRD)
Cirrhosis
Received anticoagulant medications
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Post TURP hematuria due to Asiprin consumption. Timepoint: First 28 Days after TURP. Method of measurement: Hemoglobin decline.
- Secondary Outcome Measures
Name Time Method Cardiac complication after TURP. Timepoint: First 28 days after TURP. Method of measurement: Cardiac enzyme checks in suspected cases.