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L-Arginine and Erectile Dysfunction

Oral Administration of L-Arginine in Patients With Erectile Dysfunction

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00777075
Enrollment
57
Registered
2008-10-22
Start date
2003-07-31
Completion date
2005-11-30
Last updated
2008-10-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Erectile Dysfunction

Keywords

nitrate, nitric oxide, asymmetric dimethylarginine, blood pressure, NOS, IIEF

Brief summary

The purpose of the study is to determine whether the treatment with L-arginine leads to an improvement of erectile dysfunction in patients with erectile dysfunction.

Detailed description

Erectile dysfunction (ED) is a common medical disorder often affecting the aging male. Nitric oxide (NO) is a physiological signal essential to penile erection. NO synthase (NOS) catalyzes the production of NO from L-arginine. ADMA, a competitive inhibitor of NO synthase increases with age and many disorders that reduce NO in the erectile tissue are commonly associated with ED. Although new pharmacological strategies have been identified for medical treatment of ED, patients often seek alternative therapies for cost or side effect reasons. The aim of the present study is to determine the efficacy of orally administered L-arginine on ED not caused by established organic disease.

Interventions

DRUGL-arginine
DRUGPlacebo

Sponsors

Pharmacia
CollaboratorINDUSTRY
Hannover Medical School
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
MALE
Age
20 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Patients age between 20 and 65 years, an ED for at least 6 months duration and written consent. * Each patient had to be informed about the study details in written and oral form before the beginning of the drug administration. * The hormonal status including dehydroepiandrosterone sulfate (DHEAS), Prolactin and Testosteron of each patient had to be within the normal range. -

Exclusion criteria

* Patients with primary erectile dysfunction, congenital anomalies, Diabetes mellitus, severe hepatic-and renal insufficiency, severe cardiovascular diseases, cerebrovascular accidents, uncontrolled hypertension, endocrine diseases, psychiatric disorders, and evidence of dementia were excluded. * Patients were excluded if they had pelvic fractures or prostatectomy and if they had undergone reconstructive or prosthetic surgery on the penis. * Increased levels of serum potassium, known hypersensitivity to the study medication or any ingredient of the drug. * Administration of PDE-5-Inhibitors (sildenafil, tadalafil, vardenafil or apomorphine) within four weeks prior to the administration of l-arginine or placebo led to exclusion.

Design outcomes

Primary

MeasureTime frame
International Index of Erectile Dysfunction16 weeks

Secondary

MeasureTime frame
L-arginine plasma-levels16 weeks

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026