Efficacy and Safety Study of Udenafil Tablets in Erectile Dysfunction.

Erectile Dysfunction Clinical Trial

Official title:

A Randomized, Double Blind, Placebo Controlled, Multicentric Study to Assess the Efficacy and Safety of Udenafil Tablets in Patients Suffering From Erectile Dysfunction.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01305083
• Other study ID #: AI2010-01
• Status: Completed
• Phase: Phase 3
• First received: February 25, 2011
• Last updated: May 11, 2012
• Start date: October 2010
• Est. completion date: August 2011

Study information

• Verified date: May 2012
• Source: Abdi Ibrahim Ilac San. ve Tic A.S.
• Contact: n/a
• Is FDA regulated: No
• Health authority: Turkey: Ministry of Health
• Study type: Interventional

Clinical Trial Summary

This randomized, double blind, placebo controlled, multicentric, clinical study will assess the efficacy and safety of Udenafil (100 mg) tablets in patients suffering from erectile dysfunction(ED).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 118
• Est. completion date: August 2011
• Est. primary completion date: August 2011
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

• Male patients of 18 to 60 years of age.

• Patients in a stable, monogamous sexual relationship with a female partner for at least 6 months and willing to maintain this relationship for the duration of the study.

• Patients with established diagnosis of erectile dysfunction (ED) of organic, psychogenic or mixed etiology for at least 6 months duration.

• Patient willing to attempt at least one sexual intercourse in a week for the entire treatment.

Exclusion Criteria:

• Patients with total erectile failure or any other sexual disorder such as hypoactive sexual desire.

• Patients who have previously failed to respond to PDE-5 inhibitors like Sildenafil, Vardenafil or Tadalafil.

• Patients who have used other erectile dysfunction therapies within 14 days (2 weeks) prior to entering into this study (i.e. visit 1).

• Patients with hypogonadism or anatomical deformity of the penis such as severe penile fibrosis or Peyronie's disease or penile trauma.

• Patients with a history of major psychiatric disorder.

• Patients with a history of significant pathological cardiovascular conditions such as: congestive heart failure, life-threatening arrhythmia or ischemic heart disease within the past 6 months.

• Patients with a history of central nervous system disorders such as stroke, transient ischemic attacks or spinal cord injury or a radical prostatectomy or radical pelvic surgery.

• Patients with hypotension (<90/50) or uncontrolled hypertension (>170/100), uncontrolled diabetes, hepatic impairment (SGOT or SGPT levels > 3 x Upper Normal Limit), renal impairment (serum creatinine > 2.5mg/dl), hematological disorders such as bleeding disorders.

• Patients with a history of retinitis pigmentosa, proliferative diabetic retinopathy or non-arteritic anterior ischemic optic neuropathy (NAION).

• Patients with a history of sickle cell disease, multiple myeloma, leukemia or any other disorders that may cause priapism.

• Patients on concomitant treatment with nitrates/nitrites(NO) donor, CYP3A4 inhibitors, CYP3A4 inducers, anticoagulants, androgens, antiandrogens or trazodone.

• Patients with known hypersensitivity to PDE 5 inhibitors like Sildenafil, Vardenafil or Tadalafil.

• Patient with known diagnosis to AIDS or with a positive HIV result at study screening visit.

• Patients with any other serious concurrent illness or malignancy.

• Patients with continuing history of alcohol and / or drug abuse.

• Participation in another clinical trial in the past 30days.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Erectile Dysfunction

Intervention

Drug:
• Udenafil
Placebo-control
• Placebo
Placebo

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Abdi Ibrahim Ilac San. ve Tic A.S.

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	IIEF		8 week	No
Secondary	Changes in the total score of IIEF at the end of the treatment compared to baseline.		8 week	No
Secondary	Changes in score of Question 3 (SEP2) and Question 4 (SEP3) of IIEF questionnaire at the end of the treatment period as compared to baseline.		8 week	No
Secondary	Overall assessment of efficacy (GAQ) to the study medication at the end of the study.		8 week	No