Erectile DysfunctionPhase 2/3NCT05955001
Efficacy of Tadalafil (5mg) For Treatment of Early Storage Symptoms and Erectile Dysfunction After Endoscopic Enucleation of Prostate
A Phase 2/3 study of Erectile Dysfunction and Lower Urinary Tract Symptoms, run by Mansoura University at 1 site in Egypt.
Trial summary
From previous studies, the investigators found that sexual outcomes after prostate surgery may show insignificant improvement, remain unchanged or deteriorate in non-negligible number of patients especially those with high preoperative IIEF scores. Read more about this study
- Who is it for?
- Ages 40 to 80 years
- Conditions the study is for
- Erectile Dysfunction, Lower Urinary Tract Symptoms
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 110 participants
- Where
- 1 siteEgypt
- Study dates
- 1 Apr 2023to Jul 2025
- Phase
- Phase 2/3
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 40 to 80 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- 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
Who cannot join
- 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)
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Egypt1 site, 1 recruiting
- Recruiting
Urology and Nephrology Center
Al Mansurah, Dakahlia Governorate, 35516
Nasr Eltabey, MD
About this study
Official title: A Randomized Controlled Trial to Examine the Utility of Tadalafil (5mg) For Treatment of Early Storage Symptoms and Erectile Dysfunction After Anatomical Endoscopic Enucleation of Prostate (AEEP)
From previous studies, the investigators found that sexual outcomes after prostate surgery may show insignificant improvement, remain unchanged or deteriorate in non-negligible number of patients especially those with high preoperative IIEF scores. Deterioration of erectile function could be attributed to persistence of storage symptoms specially nocturia. Several pathophysiologic mechanisms, described before, are involved in pathogenesis of LUTS and ED and one can imagine that after relief of obstruction, the erectile function should improve, however lack of improvement or even deterioration suggests that damage associated with these mechanisms is irreversible and patients may require some sort of penile rehabilitation after surgery.
The investigators hypothesized that Tadalafil may enhance relief of storage symptoms and enhance recovery of erectile function after surgery for BPH. With this assumption, a RCT was designed to examine the utility and efficacy of Tadalafil, once daily dose, to relieve persistent/ de novo storage symptoms and early erectile function deterioration after endoscopic prostate surgery.
Read the detailed description
- Introduction
Benign prostatic hyperplasia (BPH) accompanied by bothersome lower urinary tract symptoms (LUTS) is a common and progressive condition that significantly affects quality of life (QOL) in men. LUTS include storage, voiding, and post-micturition symptoms. Storage symptoms are referred as particularly bothersome and cause significant morbidity . Several population based studies demonstrated a strong association between LUTS and erectile dysfunction (ED) among BPH patients. This is believed to be independent of age and associated comorbidities like cardiovascular disease and diabetes mellitus.
Several mechanisms have been postulated to explain the relationship between LUTS and ED. First, impairment of nitric oxide (NO) production specially with conditions like hypertension and metabolic syndrome . Second, enhanced Rho/ROCK pathway that leads to impaired smooth muscle relaxation resulting in ED and LUTS. Overexpression of Rho/ROCK pathway has been found in hypertensive rats . Third, sympathetic over- activity, in particular, overexpression of α1A and α1D adrenergic receptors that are present mainly in prostate and hypertrophied detrusor muscle, respectively. Experimental studies demonstrated that hypertensive rats had increased sympathetic innervation to bladder and prostate, LUTS and ED. Furthermore, improvement of ED occurred after control of hypertension. Lastly, pelvic ischemia that results from atherosclerosis plays an important role in development of LUTS and ED via induction of fibrosis and decreased NO levels. In a cross sectional study by Berger et al , the authors found that patients with BPH and ED had lower perfusion and higher resistive index of the transition zone of prostate compared to young adults.
The main objective for treatment of BPH is to relieve LUTS and consequently improving quality of life. Anatomical endoscopic enucleation of prostate (AEEP) including, HoLEP and ThuLEP is recommended by the European Urological Association guideline as an efficient and advanced minimally invasive, size-independent surgical therapy of BPO. Their long-term efficacy, durability and safety have been proven in several prospective and randomized controlled studies .
I.1 Problems frequently encountered after AEEP that affect quality of life.
I.1.1 Persistent or De novo Storage Symptoms
Following HoLEP, a significant proportion of patients complain of persistent or even de novo storage symptoms. In a randomized trial comparing between HoLEP and TURP, Montorsi et al found that 44% of HoLEP patients experienced urgency, dysuria and urgency incontinence. Ahyai and colleagues prospectively analysed the incidence of storage symptoms after HoLEP among 144 patients. They found a significant (rebound) increase in storage symptoms at 6th and 8th week postoperatively that was attributed to the wound healing process and tissue edema. Moreover, persistence of storage symptoms led to delayed improvement in QoL that didn't significantly improved till 12 weeks after surgery when storage symptoms subsided.
Elkoushy et al compared the incidence of postoperative storage symptoms between HoLEP and PVP and found a significantly lower incidence in HoLEP group . The authors identified, baseline IPSS-storage subscore≥9, prolonged operative time>100 minutes and lower percentage of postoperative PSA reduction as independent predictors of less improvement of postoperative storage symptoms.
I.1.2. Sexual function deterioration
The impact of HoLEP on sexual function has been extensively addressed in literature with conflicting results. Some studies showed that HoLEP resulted in reduction of International Index of Erectile Function (IIEF) questionnaires postoperatively because of retrograde ejaculation that lowered IIEF orgasmic function domain . In a prospective controlled study, Elshal et al demonstrated a decline in erectile function (EF) domain after HoLEP in patients with normal preoperative EF (score >25). The authors also noted higher utilization of PDE5I from 27% to 30% at last follow up . In a retrospective study comparing effects of HoLEP, HoLAP and PVP on sexual function, the authors reported a decline in IIEF in 17% of patients after HoLEP . Higher baseline IIEF and high Energy/Prostate ratio were independent predictors of sexual function deterioration. In a recent prospective study including 144 patients treated with HoLEP, significant deterioration of IIEF for 24 weeks follow up after surgery. Jeong et al analysed serial changes in sexual function at 1,3,6 and 12 months after HoLEP and found early deterioration and return to baseline at 12 months follow up.
Theoretically, HoLEP has minimal effects on erection because of its pulsed nature, shallow depth of penetration (0.4mm) and majority of the procedure is performed with bunt dissection and laser energy is used mainly for control of blood vessels. Thus, the potential thermal effect on cavernous tissue or neurovascular bundles is minimal. Other factors could be attributed to early decline in erectile function including: anxiety after surgery, pain, postoperative complications, lack of ejaculation and bothering LUTS. Kim et al evaluated sexual outcomes after HoLEP using MSHQ and found a strong correlation between postoperative erectile function and nocturia. The authors explained their finding as decrease in nocturia led to better sleep quality and decreased overall physical fatigue thus increasing penile tumescence and erections.
I.2. Can penile rehabilitation enhance recovery of erectile function??? The concepts of penile rehabilitation has been studied after radical prostatectomy (RP) and can be defined as the use of any drug or device at or after RP to maximize erectile function recovery. Although there are different treatment methods used in penile rehabilitation, the most common approach of penile rehabilitation after RP are oral phosphodiesterase type 5 inhibitors (PDE5-I). Tadalafil is a long-acting PDE5 inhibitor (PDE5-I) that has been approved by US Food and Drug Administration (FDA) and by the European Medical Agency (EMA) for men with BPH-LUTS and for those with coexisting erectile dysfunction (ED) and BPH-LUTS. Clinical studies showed that Tadalafil improved symptoms of BPH, including both storage and voiding symptoms, in men with or without erectile dysfunction (ED).
I.3. Role of Phosphodiesterase 5 inhibitors (PDE5Is) in treatment of LUTS/ED
Mechanism of action:
PDE5 isoenzymes are highly expressed in human lower urinary tract (LUT) tissues. PDE5Is increase intracellular cyclic guanosine monophosphate (cGMP), leading to smooth muscle relaxation. The effect of PDE5 inhibition leading to elevated NO/cGMP concentration in the corpus cavernosum and pulmonary arteries has been observed, as well, in the smooth muscle of the prostate and bladder and their vascular supply. Moreover, chronic treatment with PDE5Is seems to increase blood perfusion and oxygenation in the LUT reducing chronic pelvic ischemia with its related functional and morphologic changes on bladder and prostate. PDE5I could also reduce chronic inflammation in the prostate and bladder. Nitric oxide and PDE5Is might also alter reflex pathways in the spinal cord and neurotransmission in the urethra, prostate, or bladder decreasing perception of bladder fullness and feeling of urgency.
II. Aim of the work From previous studies, we can conclude that sexual outcomes after prostate surgery may show insignificant improvement, remain unchanged or deteriorate in non-negligible number of patients especially those with high preoperative IIEF scores. Deterioration of erectile function could be attributed to persistence of storage symptoms specially nocturia. Several pathophysiologic mechanisms, described before, are involved in pathogenesis of LUTS and ED and one can imagine that after relief of obstruction, the erectile function should improve, however lack of improvement or even deterioration suggests that damage associated with these mechanisms is irreversible and patients may require some sort of penile rehabilitation after surgery.
The investigators hypothesized that Tadalafil may enhance relief of storage symptoms and enhance recovery of erectile function after surgery for BPH. With this assumption, a RCT was designed to examine the utility and efficacy of Tadalafil, once daily dose, to relieve persistent/ de novo storage symptoms and early erectile function deterioration after endoscopic prostate surgery.
Update (June 2025):
The initially listed time frame for outcome measures as "6 months" was a typographical error during registration. In practice, patients received Tadalafil or placebo for 3 months, and the primary assessment of orgasm perception (IIEF-15 domain) was conducted at 1 and 3 months while the patient was on treatment. The 6-month assessment represents post-treatment follow-up to evaluate symptom durability and resolution of postoperative recovery factors. No changes were made to outcome definitions or study design.
- Conditions
- Erectile Dysfunction, Lower Urinary Tract Symptoms
- Being tested
- Tadalafil 5mg / Placebo
- Medical subject headings
- Erectile Dysfunction, Lower Urinary Tract Symptoms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Tadalafil 5mg / PlaceboDrug
Also called Placebo
Patients after Holmium laser Enucleation of Prostate (HoLEP) will receive single daily dose of Tadalafil for 3 months and compared to Placebo
| Study group | Role | What they receive |
|---|---|---|
| Tadalafil 5 mg daily | Experimental | those patients will receive Tadalafil 5 mg daily after HoLEP Receives: Drug: Tadalafil 5mg / Placebo |
| Placebo | Experimental | Those patients will receive Placebo after HoLEP Receives: Drug: Tadalafil 5mg / Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Orgasm perception domain of International Index of Erectile Function (IIEF-15) questionnaire at 6 months among the study groups
the erectile function will be assessed using a validated questionnaire and compared to baseline .
Measured: 1 and 3 months postoperatively (during treatment), and at 6 months postoperatively (3 months after treatment cessation)
Secondary outcomes (1)
Change in International Prostate Symptom Score (IPSS) with its subdomains voiding and storage once at different follow up points.
patients in the experimental group will also be evaluated in terms of urinary symptoms and whether their irritative symptoms were improved in comparison to baseline
Measured: 2 weeks, 1, 3 months (during treatment) and at 6 months postoperatively ( 3 months after treatment cessation)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Jul 2023
- Study start1 Apr 2023
- Primary completionJul 2025 (estimated)
- Study completionJul 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Erectile DysfunctionStudies of the same condition, open and under way.
- More trials run by Mansoura UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2/3
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind
- Who is masked
- Participant, Care provider, Investigator
- Enrolment
- 110 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Mansoura University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Mahmoud Laymon, Mansoura University
- Investigators
- Mahmoud Laymon, MD,MRCS, Principal investigator, urology and nephrology center mansoura university
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05955001
- Sponsor's protocol ID
- MS.22.11.2208
- Status last verified
- Jun 2025
- First submitted
- 11 Jul 2023
- Last updated
- 11 Jun 2025
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 11 Jun 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Randomized Controlled Trial to Examine the Utility of Tadalafil (5mg) For Treatment of Early Storage Symptoms and Erectile Dysfunction After Anatomical Endoscopic Enucleation of Prostate (AEEP)
- ClinicalTrials.gov ID
- NCT05955001
- Acronym / sponsor ID
- MS.22.11.2208
- Conditions
- Erectile Dysfunction, Lower Urinary Tract Symptoms
- Phase
- Phase 2/3
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 110 participants (estimated)
- Lead sponsor
- Mansoura UniversityUniversity, hospital or other
- Study start
- 1 Apr 2023 (actual)
- Primary completion
- Jul 2025 (estimated)
- Study completion
- Jul 2025 (estimated)
- First posted
- 20 Jul 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
From previous studies, the investigators found that sexual outcomes after prostate surgery may show insignificant improvement, remain unchanged or deteriorate in non-negligible number of patients especially those with high preoperative IIEF scores. Deterioration of erectile function could be attributed to persistence of storage symptoms specially nocturia. Several pathophysiologic mechanisms, described before, are involved in pathogenesis of LUTS and ED and one can imagine that after relief of obstruction, the erectile function should improve, however lack of improvement or even deterioration suggests that damage associated with these mechanisms is irreversible and patients may require some sort of penile rehabilitation after surgery.
The investigators hypothesized that Tadalafil may enhance relief of storage symptoms and enhance recovery of erectile function after surgery for BPH. With this assumption, a RCT was designed to examine the utility and efficacy of Tadalafil, once daily dose, to relieve persistent/ de novo storage symptoms and early erectile function deterioration after endoscopic prostate surgery.
Detailed description
- Introduction
Benign prostatic hyperplasia (BPH) accompanied by bothersome lower urinary tract symptoms (LUTS) is a common and progressive condition that significantly affects quality of life (QOL) in men. LUTS include storage, voiding, and post-micturition symptoms. Storage symptoms are referred as particularly bothersome and cause significant morbidity . Several population based studies demonstrated a strong association between LUTS and erectile dysfunction (ED) among BPH patients. This is believed to be independent of age and associated comorbidities like cardiovascular disease and diabetes mellitus.
Several mechanisms have been postulated to explain the relationship between LUTS and ED. First, impairment of nitric oxide (NO) production specially with conditions like hypertension and metabolic syndrome . Second, enhanced Rho/ROCK pathway that leads to impaired smooth muscle relaxation resulting in ED and LUTS. Overexpression of Rho/ROCK pathway has been found in hypertensive rats . Third, sympathetic over- activity, in particular, overexpression of α1A and α1D adrenergic receptors that are present mainly in prostate and hypertrophied detrusor muscle, respectively. Experimental studies demonstrated that hypertensive rats had increased sympathetic innervation to bladder and prostate, LUTS and ED. Furthermore, improvement of ED occurred after control of hypertension. Lastly, pelvic ischemia that results from atherosclerosis plays an important role in development of LUTS and ED via induction of fibrosis and decreased NO levels. In a cross sectional study by Berger et al , the authors found that patients with BPH and ED had lower perfusion and higher resistive index of the transition zone of prostate compared to young adults.
The main objective for treatment of BPH is to relieve LUTS and consequently improving quality of life. Anatomical endoscopic enucleation of prostate (AEEP) including, HoLEP and ThuLEP is recommended by the European Urological Association guideline as an efficient and advanced minimally invasive, size-independent surgical therapy of BPO. Their long-term efficacy, durability and safety have been proven in several prospective and randomized controlled studies .
I.1 Problems frequently encountered after AEEP that affect quality of life.
I.1.1 Persistent or De novo Storage Symptoms
Following HoLEP, a significant proportion of patients complain of persistent or even de novo storage symptoms. In a randomized trial comparing between HoLEP and TURP, Montorsi et al found that 44% of HoLEP patients experienced urgency, dysuria and urgency incontinence. Ahyai and colleagues prospectively analysed the incidence of storage symptoms after HoLEP among 144 patients. They found a significant (rebound) increase in storage symptoms at 6th and 8th week postoperatively that was attributed to the wound healing process and tissue edema. Moreover, persistence of storage symptoms led to delayed improvement in QoL that didn't significantly improved till 12 weeks after surgery when storage symptoms subsided.
Elkoushy et al compared the incidence of postoperative storage symptoms between HoLEP and PVP and found a significantly lower incidence in HoLEP group . The authors identified, baseline IPSS-storage subscore≥9, prolonged operative time>100 minutes and lower percentage of postoperative PSA reduction as independent predictors of less improvement of postoperative storage symptoms.
I.1.2. Sexual function deterioration
The impact of HoLEP on sexual function has been extensively addressed in literature with conflicting results. Some studies showed that HoLEP resulted in reduction of International Index of Erectile Function (IIEF) questionnaires postoperatively because of retrograde ejaculation that lowered IIEF orgasmic function domain . In a prospective controlled study, Elshal et al demonstrated a decline in erectile function (EF) domain after HoLEP in patients with normal preoperative EF (score >25). The authors also noted higher utilization of PDE5I from 27% to 30% at last follow up . In a retrospective study comparing effects of HoLEP, HoLAP and PVP on sexual function, the authors reported a decline in IIEF in 17% of patients after HoLEP . Higher baseline IIEF and high Energy/Prostate ratio were independent predictors of sexual function deterioration. In a recent prospective study including 144 patients treated with HoLEP, significant deterioration of IIEF for 24 weeks follow up after surgery. Jeong et al analysed serial changes in sexual function at 1,3,6 and 12 months after HoLEP and found early deterioration and return to baseline at 12 months follow up.
Theoretically, HoLEP has minimal effects on erection because of its pulsed nature, shallow depth of penetration (0.4mm) and majority of the procedure is performed with bunt dissection and laser energy is used mainly for control of blood vessels. Thus, the potential thermal effect on cavernous tissue or neurovascular bundles is minimal. Other factors could be attributed to early decline in erectile function including: anxiety after surgery, pain, postoperative complications, lack of ejaculation and bothering LUTS. Kim et al evaluated sexual outcomes after HoLEP using MSHQ and found a strong correlation between postoperative erectile function and nocturia. The authors explained their finding as decrease in nocturia led to better sleep quality and decreased overall physical fatigue thus increasing penile tumescence and erections.
I.2. Can penile rehabilitation enhance recovery of erectile function??? The concepts of penile rehabilitation has been studied after radical prostatectomy (RP) and can be defined as the use of any drug or device at or after RP to maximize erectile function recovery. Although there are different treatment methods used in penile rehabilitation, the most common approach of penile rehabilitation after RP are oral phosphodiesterase type 5 inhibitors (PDE5-I). Tadalafil is a long-acting PDE5 inhibitor (PDE5-I) that has been approved by US Food and Drug Administration (FDA) and by the European Medical Agency (EMA) for men with BPH-LUTS and for those with coexisting erectile dysfunction (ED) and BPH-LUTS. Clinical studies showed that Tadalafil improved symptoms of BPH, including both storage and voiding symptoms, in men with or without erectile dysfunction (ED).
I.3. Role of Phosphodiesterase 5 inhibitors (PDE5Is) in treatment of LUTS/ED
Mechanism of action:
PDE5 isoenzymes are highly expressed in human lower urinary tract (LUT) tissues. PDE5Is increase intracellular cyclic guanosine monophosphate (cGMP), leading to smooth muscle relaxation. The effect of PDE5 inhibition leading to elevated NO/cGMP concentration in the corpus cavernosum and pulmonary arteries has been observed, as well, in the smooth muscle of the prostate and bladder and their vascular supply. Moreover, chronic treatment with PDE5Is seems to increase blood perfusion and oxygenation in the LUT reducing chronic pelvic ischemia with its related functional and morphologic changes on bladder and prostate. PDE5I could also reduce chronic inflammation in the prostate and bladder. Nitric oxide and PDE5Is might also alter reflex pathways in the spinal cord and neurotransmission in the urethra, prostate, or bladder decreasing perception of bladder fullness and feeling of urgency.
II. Aim of the work From previous studies, we can conclude that sexual outcomes after prostate surgery may show insignificant improvement, remain unchanged or deteriorate in non-negligible number of patients especially those with high preoperative IIEF scores. Deterioration of erectile function could be attributed to persistence of storage symptoms specially nocturia. Several pathophysiologic mechanisms, described before, are involved in pathogenesis of LUTS and ED and one can imagine that after relief of obstruction, the erectile function should improve, however lack of improvement or even deterioration suggests that damage associated with these mechanisms is irreversible and patients may require some sort of penile rehabilitation after surgery.
The investigators hypothesized that Tadalafil may enhance relief of storage symptoms and enhance recovery of erectile function after surgery for BPH. With this assumption, a RCT was designed to examine the utility and efficacy of Tadalafil, once daily dose, to relieve persistent/ de novo storage symptoms and early erectile function deterioration after endoscopic prostate surgery.
Update (June 2025):
The initially listed time frame for outcome measures as "6 months" was a typographical error during registration. In practice, patients received Tadalafil or placebo for 3 months, and the primary assessment of orgasm perception (IIEF-15 domain) was conducted at 1 and 3 months while the patient was on treatment. The 6-month assessment represents post-treatment follow-up to evaluate symptom durability and resolution of postoperative recovery factors. No changes were made to outcome definitions or study design.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, care provider, investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Tadalafil 5 mg daily | Experimental | Drug: Tadalafil 5mg / Placebothose patients will receive Tadalafil 5 mg daily after HoLEP |
| Placebo | Experimental | Drug: Tadalafil 5mg / PlaceboThose patients will receive Placebo after HoLEP |
Who may qualify
- Ages
- 40 to 80 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- 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.
Key exclusion criteria (5 listed)
- 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)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Tadalafil 5mg / PlaceboAlso: PlaceboPatients after Holmium laser Enucleation of Prostate (HoLEP) will receive single daily dose of Tadalafil for 3 months and compared to Placebo | Drug | Placebo, Tadalafil 5 mg daily |
Primary outcome
Orgasm perception domain of International Index of Erectile Function (IIEF-15) questionnaire at 6 months among the study groups
Time frame: 1 and 3 months postoperatively (during treatment), and at 6 months postoperatively (3 months after treatment cessation)
the erectile function will be assessed using a validated questionnaire and compared to baseline .
1 secondary outcome
Change in International Prostate Symptom Score (IPSS) with its subdomains voiding and storage once at different follow up points.
Time frame: 2 weeks, 1, 3 months (during treatment) and at 6 months postoperatively ( 3 months after treatment cessation)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Jun 2025.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Mahmoud Laymon, MD,MRCS principal investigator
urology and nephrology center mansoura university
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2/3 study of Erectile Dysfunction and Lower Urinary Tract Symptoms, run by Mansoura University at 1 site in Egypt.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 11 Jun 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this combined phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Mahmoud Laymon, MD,MRCS (01002275698, dr_mahmoudlaymon@mans.edu.eg), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Orgasm perception domain of International Index of Erectile Function (IIEF-15) questionnaire at 6 months among the study groups (time frame: 1 and 3 months postoperatively (during treatment), and at 6 months postoperatively (3 months after treatment cessation)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Jun 2025.