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Completed

NCT Number: NCT00421460

The Therapy of Nebido as Mono or in Combination With PDE-5 Inhibitors in Hypogonadal Patients With Erectile Dysfunction

The purpose of this study is to evaluate the response of a treatment with testosterone undecanoate and determine the levels of total and free testosterone in hypogonadal patients with erectile dysfunction.

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Key information

Age range

18 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Phase 4

Primary location

Siriraj Hospital, Bangkoknoi, Bangkok, Thailand

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About this study

Hypogonadism is a pathophysiologic and clinical factor in a substantial number of patients with ED,and data indicate that a threshold level of testosterone is necessary for normal erectile function.Testosterone therapy is clearly indicated in hypogonadal patients and is beneficial in other patients with ED and hypogonadism.However,testosterone efficacy as monotherapy for ED could be limited,and combination therapy with testosterone and other ED treatments,such as PDE-5 inhibitors may be valuable in certain subpopulations of patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with ED over 3 months (specify using IIEF score)
  • Age >= 18 years.
  • Stable sexual relationship
  • With low or low normal serum testosterone level (either total or bioavailable testosterone) TT <= 4 ng/ml and/or BT <= 1 ng/ml
  • Aging Male Symptom scale with total score starting at 37 points (must not replace TT < 4 ng/ml)
  • Eligible subjects who previously took the oral androgen or PDE5 inhibitor must have discontinued their use for 1 month

Exclusion criteria

  • Contraindication to treatment with Testosterone according to the SPC
  • Hypersensitivity to the active substances or any of the excipients of Nebido
  • Diagnosed or suspected carcinoma of the prostate or the male breast cancer
  • Past or present liver tumors
  • Acute or chronic hepatic diseases
  • Severe cardiac, hepatic or renal insufficiency
  • History of penile implant or significant penile deformity
  • Diagnosed sleep apnea
  • Polycythemia (Hematocrit >50%)
  • Prolactin >25 ng/ml
  • Organic hypothalamic-pituitary pathology
  • Any unstable medical, psychiatric or drug/alcohol abuse disorder
  • Prostate specific antigen (PSA)>= 4 ng/ml
  • Severe symptomatic benign prostatic hyperplasia (IPSS) sum score >=20)
  • Diabetes mellitus which is uncontrolled (HbAlc level >10%)
  • Epilepsy not adequately controlled by treatment
  • Patients requiring fertility treatment
  • Hypertension which is not adequately controlled on therapy
  • Clinically significant chronic hematological disease which may lead to priapism such as sickle cell anemia, multiple myeloma or leukemia
  • Hypersensitivity to PDE-5 inhibitors
  • Concomitant Medication:
  • Nitrites or Nitric oxide donors
  • Anti-androgens
  • anti-coagulants, with the exception of anti-platelet agents
  • Any of potent inhibitors of cytochrome P-450 3A4:such as HIV protease inhibitors (Ritonavir or Indinavir); Anti-mycotic agent (Itraconazole and Ketoconazole)-topical application allowed; or Erythromycin.

Treatment and study plan

Testosterone Undecanoate,1000mg

Drug

duration for 4 injections

Other names: Nebido 1000 mg

Primary outcomes

  1. Response of treatment for 4 injections at 1 year; score on an IIEF-5

    Time frame: 4 injections at 1 year for each subject, at 12,30,46 weeks.

Secondary outcomes

  1. Testosterone level

    Time frame: at 6,12,18,36,46 weeks

Sponsors and collaborators

Lead sponsor

Chulalongkorn University

Other

Collaborators

  • Ramathibodi Hospital
  • Siriraj Hospital

Registry information

Official study title

Phase IV Study of The Therapy of Long-acting Testosterone Undecanoate,1000mg in 4 ml Oily Solution for i.m.Injection(Nebido) as Mono or in Combination With PDE-5 Inhibitors in Hypogonadal Patients With Erectile Dysfunction

Important dates

Study start
2007
Primary completion
2011
Study completion
2011
First posted
Jan 12, 2007
Registry last updated
May 15, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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