The Therapy of Nebido as Mono or in Combination With PDE-5 Inhibitors in Hypogonadal Patients With Erectile Dysfunction
NCT ID: NCT00421460
Last Updated: 2012-05-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE4
30 participants
INTERVENTIONAL
2007-01-31
2011-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Interventions
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Testosterone Undecanoate,1000mg
duration for 4 injections
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. Age \>= 18 years.
3. Stable sexual relationship
4. With low or low normal serum testosterone level (either total or bioavailable testosterone) TT \<= 4 ng/ml and/or BT \<= 1 ng/ml
5. Aging Male Symptom scale with total score starting at 37 points (must not replace TT \< 4 ng/ml)
6. Eligible subjects who previously took the oral androgen or PDE5 inhibitor must have discontinued their use for 1 month
Exclusion Criteria
2. Hypersensitivity to the active substances or any of the excipients of Nebido
3. Diagnosed or suspected carcinoma of the prostate or the male breast cancer
4. Past or present liver tumors
5. Acute or chronic hepatic diseases
6. Severe cardiac, hepatic or renal insufficiency
7. History of penile implant or significant penile deformity
8. Diagnosed sleep apnea
9. Polycythemia (Hematocrit \>50%)
10. Prolactin \>25 ng/ml
11. Organic hypothalamic-pituitary pathology
12. Any unstable medical, psychiatric or drug/alcohol abuse disorder
13. Prostate specific antigen (PSA)\>= 4 ng/ml
14. Severe symptomatic benign prostatic hyperplasia (IPSS) sum score \>=20)
15. Diabetes mellitus which is uncontrolled (HbAlc level \>10%)
16. Epilepsy not adequately controlled by treatment
17. Patients requiring fertility treatment
18. Hypertension which is not adequately controlled on therapy
19. Clinically significant chronic hematological disease which may lead to priapism such as sickle cell anemia, multiple myeloma or leukemia
20. Hypersensitivity to PDE-5 inhibitors
21. 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.
18 Years
MALE
No
Sponsors
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Ramathibodi Hospital
OTHER
Siriraj Hospital
OTHER
Chulalongkorn University
OTHER
Responsible Party
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Principal Investigators
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Apichat Kongkanand, Professor
Role: PRINCIPAL_INVESTIGATOR
King Chulalongkorn Memmorial Hospital
Locations
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Siriraj Hospital
Bangkoknoi, Bangkok, Thailand
Ramathibodi Hospital
Rajthevee, Bangkok, Thailand
King Chulalongkorn Memorial Hospital
Bangkok, , Thailand
Countries
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Other Identifiers
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TH 023101
Identifier Type: -
Identifier Source: org_study_id
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