AzTrials
AzTrials

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.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

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.

Egypt1 site
  • Mohamed Mahmoud Dogha

    Al Fayyum, Keman Fares, 63514

Other trials in Egypt

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.

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 groups in NCT06947265
Study groupRoleWhat they receive
Group AExperimentalwas given daily 3 g(three divided doses) oral tablets of L-arginine for eight weeks
Receives: Drug: L-Arginine
Group BExperimentalwas given daily 5 mg oral tablets of Tadalafil for eight weeks.
Receives: Drug: Tadalafil 5 mg
Group CExperimentalwas 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.

  1. 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)
  1. testosterone level

    androgenic hormone changes in response to treatment

    Measured: 8 weeks of treatment

  2. 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.

  1. First posted27 Apr 2025
  2. Study start14 Jan 2024
  3. Primary completion1 Jan 2025
  4. Study completion1 Feb 2025

Resources

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)
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

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.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in