Efficacy of Tadalafil (5mg) For Treatment of Early Storage Symptoms and Erectile Dysfunction After Endoscopic Enucleation of Prostate
Erectile Dysfunction, Lower Urinary Tract Symptoms
About this trial
This is an interventional prevention trial for Erectile Dysfunction
Eligibility Criteria
Inclusion Criteria: Patients' age ≥ 40 years LUTS secondary to BOO due to BPH who failed medical treatment International prostate symptom scores (IPSS) >15 and bother score (QOL) ≥ 3 (according to IPSS question 8) Peak urinary flow rate (Qmax) <15 ml/sec. ASA (American society of anaesthesiologists) score ≤ 3. Sexually active men, not receiving PDE5I Exclusion Criteria: Patients using nitrates, potassium channel opener, or α1-blockers doxazosin and terazosin for control of hypertension Patients with unstable angina pectoris, recent myocardial infarction or stroke myocardial insufficiency. Patients with severe hepatic or renal insufficiency. Patients who are sexually inactive. Patients with uncontrolled diabetes mellitus or neurologic condition(eg. parkinsoism)
Sites / Locations
- Urology and Nephrology Center
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Tadalafil 5 mg daily after AEEP
Control group with no Tadalafil
those patients will receive Tadalafil 5 mg daily after AEEP
Those patients will not receive Tadalafil after surgery