Erectile DysfunctionsPhase 4NCT06947265
Safety And Efficacy Of L-Arginine Monotherapy Versus Tadalafil Monotherapy Versus Their Combination In Men With Erectile Dysfunction; A Prospective Randomized Study
A Phase 4 study testing L-Arginine and Tadalafil 5 mg in people with Erectile Dysfunctions, run by Fayoum University Hospital at 1 site in Egypt.
Trial summary
Introduction Sexual dysfunctions are annoying health problems with the erectile problems forming the main part of them. Erectile dysfunction (ED) is defined as the persistent inability to obtain or maintain an erection that is sufficient to allow satisfactory sexual intercourse.[1] Aim of Work To evaluate the role of… Read more about this study
- Who is it for?
- Ages 45 to 75 years, men only
- Conditions the study is for
- Erectile Dysfunctions
- What is being tested?
- L-Arginine and Tadalafil 5 mg
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 180 participants
- Where
- 1 siteEgypt
- Study dates
- 14 Jan 2024to 1 Feb 2025
- Phase
- Phase 4
- Are there results?
- None posted in the registry
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 45 to 75 years
- Men only
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- • Naive ( not previously treated) male patient with mild to moderate ED according to SHIM Questionnaire.
Who cannot join
- ● Kidney disease or liver failure
- Coronary heart disease
- Peyronie's disease
- Neurological disease that may related to ED
Trial locations and contacts
1 site in 1 country.
About this study
Introduction Sexual dysfunctions are annoying health problems with the erectile problems forming the main part of them. Erectile dysfunction (ED) is defined as the persistent inability to obtain or maintain an erection that is sufficient to allow satisfactory sexual intercourse.[1] Aim of Work To evaluate the role of L-arginine monotherapy versus Tadalafil monotherapy versus their combination for the treatment of erectile dysfunction .
Patients and methods:
Read more
Inclusion criteria:
- Naive ( not previously treated) male patient with mild to moderate ED according to SHIM Questionnaire.
Exclusion criteria:
- Kidney disease or liver failure
- Coronary heart disease
- Peyronie's disease
- Neurological disease that may related to ED
Read the detailed description
Safety And Efficacy Of L-Arginine Monotherapy Versus Tadalafil Monotherapy Versus Their Combination In Men With Erectile Dysfunction; A Prospective Randomized Study
Introduction Sexual dysfunctions are annoying health problems with the erectile problems forming the main part of them. Erectile dysfunction (ED) is defined as the persistent inability to obtain or maintain an erection that is sufficient to allow satisfactory sexual intercourse.[1] It is difficult to obtain accurate values for the true prevalence of erectile dysfunction, as many patients fail to seek any medical attention The best available data according to the Massachusetts Male Aging Study indicates that 52% of males between 40 and 70 years of age are affected with erectile problems, and about 70% of males are having some subjective issues with erections at the age of 70 years.[2] Erection is a neurovascular event in which a key mediator is nitric oxide (NO). It has been shown that there is reduced NO bioactivity in ED.[3] Oral phosphodiesterase-5 inhibitors (PDE-5 inhibitors), such as sildenafil and Tadalafil, are usually the first-line treatment of erectile dysfunction. They are effective in a wide range of etiologies including cardiovascular disease, diabetes, and hypogonadism. They act by decreasing the degradation of cyclic GMP via phosphodiesterase inhibition, which increases the relaxation of cavernosal smooth muscle and cavernosal arterial blood flow. It is important to note that PDE-5 inhibitors do not initiate the erectile response. Sexual stimulation is required to release nitric oxide from the vascular endothelium and penile nerve endings to commence the erectile process. PDE-5 inhibitors are highly effective and have an overall success rate of up to 76%.[4]
As L-arginine is a natural precursor of NO and its good availability is understood to have positive effect on NO production. Data regarding the pattern of use of L-arginine for sexual problems, which is considered one of the more widely used alternatives or adjuncts to regular drugs used in the patients of ED.[5] Aim of Work To evaluate the role of L-arginine monotherapy versus Tadalafil monotherapy versus their combination for the treatment of erectile dysfunction .
Patients and methods This clinical prospective study will be carried out on patients attending urology clinic in Fayoum University Hospital with ED
Sample size :
Inclusion criteria:
- Naive ( not previously treated) male patient with mild to moderate ED according to SHIM Questionnaire.
Exclusion criteria:
- Kidney disease or liver failure
- Coronary heart disease
- Peyronie's disease
- Neurological disease that may related to ED Patients were randomized equally categorized into three treatment groups. All the patients were blinded regarding the nature of the received medications.
Group (1) was given daily 3 g(three divided doses) oral tablets of L-arginine for eight weeks.
Group (2) was given daily 5 mg oral tablets of Tadalafil for eight weeks. Group (3) was given daily 3 g oral tablets of L-arginine and 5 mg oral tablets of Tadalafil for eight weeks.
Patients were advised to practice intercourse twice to three times weekly. They were assessed before and after eight weeks of treatment Pretreatment assessment
- History taking: including medical and surgical history.
- Sexual history: onset and duration of ED and Sexual health inventory for men (SHIM) to evaluate severity of ED.
- BMI
- General medical and local genital examinations.
- LABORATORY INVESTIGATIONS:
After 12 hours of fasting, venous blood samples were drawn from all included patients before and at the end of eight weeks of treatment for total serum testosterone assessments between 8.00 and 12.00 am.
- Penile ultrasonography: Shear Wave Elastography (SWE): is a current radiologic modality can measure biologic tissue elasticity and gives elastogram which superimposed on the B-mode ultrasound which expresses tissue stiffness in numbers(kpasc)
Follow up assessment:
- First follow up visit is scheduled after one week :to evaluate any adverse effect from the treatment
- 2nd follow up visit after 8 weeks : Reassessment to the SHIM questionnaire and serum testosterone and SWE.
Statistical analysis Data from the 3 groups will be collected, compared and statistically analyzed.
- Conditions
- Erectile Dysfunctions
- Being tested
- L-Arginine, Tadalafil 5 mg
- Keywords
- erectile dysfunction , L-arginine , elastography
- Medical subject headings
- Erectile Dysfunction
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
L-ArginineDrug
get 3 gm oral tablets of L-arginine
Tadalafil 5 mgDrug
get 5 mg oral tadalafil for 8 weeks
| Study group | Role | What they receive |
|---|---|---|
| Group A | Experimental | was given daily 3 g(three divided doses) oral tablets of L-arginine for eight weeks Receives: Drug: L-Arginine |
| Group B | Experimental | was given daily 5 mg oral tablets of Tadalafil for eight weeks. Receives: Drug: Tadalafil 5 mg |
| Group C | Experimental | was given daily 3 g oral tablets of L-arginine and 5 mg oral tablets of Tadalafil for eight weeks. Receives: Drug: L-Arginine; Drug: Tadalafil 5 mg |
What is being measured
The primary outcome is the main question the study is designed to answer.
SHIM questionnaire
The SHIM (Sexual Health Inventory for Men) questionnaire is a commonly used tool for assessing erectile dysfunction (ED) in men. It is a brief, self-administered questionnaire that typically consists of five questions, with answers scored on a scale to help determine the severity of erectile dysfunction. The SHIM is widely used in both clinical practice and research to assess sexual health and function.
Here are the key elements of the SHIM:
Frequency of sexual activity (often using a scale from "almost never or never" to "almost always or always").
Confidence in maintaining an erection (again, on a similar scale). Ability to achieve an erection. Erection firmness (whether the erection is hard enough for penetration). Satisfaction with the firmness of the erection.
The scores are typically aggregated into one overall score, and depending on the score, it classifies the degree of erectile dysfunction:
25-22: No erectile dysfunction 21-17: Mild erectile dysfunction 16-12: Mild to mod
Measured: 8 weeks of treatment
Secondary outcomes (2)
testosterone level
androgenic hormone changes in response to treatment
Measured: 8 weeks of treatment
Shear Wave Elastography
a current radiologic modality can measure biologic tissue elasticity and gives elastogram which superimposed on the B-mode ultrasound which expresses tissue stiffness in numbers(kpasc)
Measured: 8 weeks of treatment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Apr 2025
- Study start14 Jan 2024
- Primary completion1 Jan 2025
- Study completion1 Feb 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Erectile DysfunctionsStudies of the same condition, open and under way.
- 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 4
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Group (1) was given daily 3 g(three divided doses) oral tablets of L-arginine for eight weeks. Group (2) was given daily 5 mg oral tablets of Tadalafil for eight weeks. Group (3) was given daily 3 g oral tablets of L-arginine and 5 mg oral tablets of Tadalafil for eight weeks.
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 180 participants (actual)
Sponsor and investigators
- Lead sponsor
- Fayoum University Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Mohamed Mahmoud Dogha, Fayoum University Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06947265
- Sponsor's protocol ID
- D 355
- Status last verified
- Apr 2025
- First submitted
- 21 Apr 2025
- Last updated
- 27 Apr 2025
- Results posted
- No
- Data monitoring committee
- Yes
- 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 27 Apr 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Safety And Efficacy Of L-Arginine Monotherapy Versus Tadalafil Monotherapy Versus Their Combination In Men With Erectile Dysfunction; A Prospective Randomized Study
- ClinicalTrials.gov ID
- NCT06947265
- Acronym / sponsor ID
- D 355
- Conditions
- Erectile Dysfunctions
- Keywords
- erectile dysfunction , L-arginine , elastography
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 180 participants (actual)
- Lead sponsor
- Fayoum University HospitalUniversity, hospital or other
- Study start
- 14 Jan 2024 (actual)
- Primary completion
- 1 Jan 2025 (actual)
- Study completion
- 1 Feb 2025 (actual)
- First posted
- 27 Apr 2025 (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.
Introduction Sexual dysfunctions are annoying health problems with the erectile problems forming the main part of them. Erectile dysfunction (ED) is defined as the persistent inability to obtain or maintain an erection that is sufficient to allow satisfactory sexual intercourse.[1] Aim of Work To evaluate the role of L-arginine monotherapy versus Tadalafil monotherapy versus their combination for the treatment of erectile dysfunction .
Patients and methods:
Inclusion criteria:
- Naive ( not previously treated) male patient with mild to moderate ED according to SHIM Questionnaire.
Exclusion criteria:
- Kidney disease or liver failure
- Coronary heart disease
- Peyronie's disease
- Neurological disease that may related to ED
Detailed description
Safety And Efficacy Of L-Arginine Monotherapy Versus Tadalafil Monotherapy Versus Their Combination In Men With Erectile Dysfunction; A Prospective Randomized Study
Introduction Sexual dysfunctions are annoying health problems with the erectile problems forming the main part of them. Erectile dysfunction (ED) is defined as the persistent inability to obtain or maintain an erection that is sufficient to allow satisfactory sexual intercourse.[1] It is difficult to obtain accurate values for the true prevalence of erectile dysfunction, as many patients fail to seek any medical attention The best available data according to the Massachusetts Male Aging Study indicates that 52% of males between 40 and 70 years of age are affected with erectile problems, and about 70% of males are having some subjective issues with erections at the age of 70 years.[2] Erection is a neurovascular event in which a key mediator is nitric oxide (NO). It has been shown that there is reduced NO bioactivity in ED.[3] Oral phosphodiesterase-5 inhibitors (PDE-5 inhibitors), such as sildenafil and Tadalafil, are usually the first-line treatment of erectile dysfunction. They are effective in a wide range of etiologies including cardiovascular disease, diabetes, and hypogonadism. They act by decreasing the degradation of cyclic GMP via phosphodiesterase inhibition, which increases the relaxation of cavernosal smooth muscle and cavernosal arterial blood flow. It is important to note that PDE-5 inhibitors do not initiate the erectile response. Sexual stimulation is required to release nitric oxide from the vascular endothelium and penile nerve endings to commence the erectile process. PDE-5 inhibitors are highly effective and have an overall success rate of up to 76%.[4]
As L-arginine is a natural precursor of NO and its good availability is understood to have positive effect on NO production. Data regarding the pattern of use of L-arginine for sexual problems, which is considered one of the more widely used alternatives or adjuncts to regular drugs used in the patients of ED.[5] Aim of Work To evaluate the role of L-arginine monotherapy versus Tadalafil monotherapy versus their combination for the treatment of erectile dysfunction .
Patients and methods This clinical prospective study will be carried out on patients attending urology clinic in Fayoum University Hospital with ED
Sample size :
Inclusion criteria:
- Naive ( not previously treated) male patient with mild to moderate ED according to SHIM Questionnaire.
Exclusion criteria:
- Kidney disease or liver failure
- Coronary heart disease
- Peyronie's disease
- Neurological disease that may related to ED Patients were randomized equally categorized into three treatment groups. All the patients were blinded regarding the nature of the received medications.
Group (1) was given daily 3 g(three divided doses) oral tablets of L-arginine for eight weeks.
Group (2) was given daily 5 mg oral tablets of Tadalafil for eight weeks. Group (3) was given daily 3 g oral tablets of L-arginine and 5 mg oral tablets of Tadalafil for eight weeks.
Patients were advised to practice intercourse twice to three times weekly. They were assessed before and after eight weeks of treatment Pretreatment assessment
- History taking: including medical and surgical history.
- Sexual history: onset and duration of ED and Sexual health inventory for men (SHIM) to evaluate severity of ED.
- BMI
- General medical and local genital examinations.
- LABORATORY INVESTIGATIONS:
After 12 hours of fasting, venous blood samples were drawn from all included patients before and at the end of eight weeks of treatment for total serum testosterone assessments between 8.00 and 12.00 am.
- Penile ultrasonography: Shear Wave Elastography (SWE): is a current radiologic modality can measure biologic tissue elasticity and gives elastogram which superimposed on the B-mode ultrasound which expresses tissue stiffness in numbers(kpasc)
Follow up assessment:
- First follow up visit is scheduled after one week :to evaluate any adverse effect from the treatment
- 2nd follow up visit after 8 weeks : Reassessment to the SHIM questionnaire and serum testosterone and SWE.
Statistical analysis Data from the 3 groups will be collected, compared and statistically analyzed.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 3
- Model description
- Group (1) was given daily 3 g(three divided doses) oral tablets of L-arginine for eight weeks. Group (2) was given daily 5 mg oral tablets of Tadalafil for eight weeks. Group (3) was given daily 3 g oral tablets of L-arginine and 5 mg oral tablets of Tadalafil for eight weeks.
| Arm | Type | Receives |
|---|---|---|
| Group A | Experimental | Drug: L-Argininewas given daily 3 g(three divided doses) oral tablets of L-arginine for eight weeks |
| Group B | Experimental | Drug: Tadalafil 5 mgwas given daily 5 mg oral tablets of Tadalafil for eight weeks. |
| Group C | Experimental | Drug: L-Arginine, Drug: Tadalafil 5 mgwas given daily 3 g oral tablets of L-arginine and 5 mg oral tablets of Tadalafil for eight weeks. |
Who may qualify
- Ages
- 45 to 75 years
- Sex
- Male only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- • Naive ( not previously treated) male patient with mild to moderate ED according to SHIM Questionnaire.
Key exclusion criteria (4 listed)
- ● Kidney disease or liver failure
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 |
|---|---|---|
| L-Arginineget 3 gm oral tablets of L-arginine | Drug | Group A, Group C |
| Tadalafil 5 mgget 5 mg oral tadalafil for 8 weeks | Drug | Group B, Group C |
Primary outcome
SHIM questionnaire
Time frame: 8 weeks of treatment
The SHIM (Sexual Health Inventory for Men) questionnaire is a commonly used tool for assessing erectile dysfunction (ED) in men. It is a brief, self-administered questionnaire that typically consists of five questions, with answers scored on a scale to help determine the severity of erectile dysfunction. The SHIM is widely used in both clinical practice and research to assess sexual health and function. Here are the key elements of the SHIM: Frequency of sexual activity (often using a scale from "almost never or never" to "almost always or always"). Confidence in maintaining an erection (again, on a similar scale). Ability to achieve an erection. Erection firmness (whether the erection is hard enough for penetration). Satisfaction with the firmness of the erection. The scores are typically aggregated into one overall score, and depending on the score, it classifies the degree of erectile dysfunction: 25-22: No erectile dysfunction 21-17: Mild erectile dysfunction 16-12: Mild to mod
2 secondary outcomes
testosterone level
Time frame: 8 weeks of treatment
Shear Wave Elastography
Time frame: 8 weeks of treatment
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Apr 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. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing L-Arginine and Tadalafil 5 mg in people with Erectile Dysfunctions, run by Fayoum University Hospital 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 1 inclusion and 4 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: finished, as of the sponsor's last update on 27 Apr 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 phase mean?
Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
SHIM questionnaire (time frame: 8 weeks of treatment). 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 27 Apr 2025.