Comparison of two prostatectomy methods
Not Applicable
Recruiting
- Conditions
- Benign prostate hyperplasia.Hyperplasia of prostate
- Registration Number
- IRCT20180305038956N1
- Lead Sponsor
- Yazd University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Male
- Target Recruitment
- 100
Inclusion Criteria
The classical indications for prostate surgery
Patients with prostate size between 30 and 70 grams
Complete the informed consent form by the patient
Exclusion Criteria
Previous prostate surgery with high PSA (Prostate Specific Antigen) Levels
Uncontrolled diabetes
History of CVA (cerebral vascular accident) and neurological diseases
Urinary tract obstruction
Addiction
Use of neurological and anticholinergic drugs
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Benign prostatic hyperplasia. Timepoint: One week after surgery, then one month, 3 months and 6 months after surgery. Method of measurement: The amount of Q-Max (Maximum urinary flow) in the uroflowmetry before and after the surgery.
- Secondary Outcome Measures
Name Time Method Bleeding. Timepoint: During surgery, up to a week later. Method of measurement: The rate of receiving blood during and after surgery, and expert examination.;Wound infection. Timepoint: One week after surgery, then up to 1 month after surgery. Method of measurement: Expert examination.;Duration of catheterization after surgery. Timepoint: 1,3,7 days after surgery. Method of measurement: Expert examination.;Urethral stricture. Timepoint: 1 week, 1 month and 3 months after surgery. Method of measurement: Expert examination and retrograde urethrography.