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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01249703
Other study ID # Chunhua Deng
Secondary ID
Status Recruiting
Phase N/A
First received November 29, 2010
Last updated November 29, 2010
Start date January 2008
Est. completion date January 2020

Study information

Verified date January 2008
Source Sun Yat-sen University
Contact Chunhua Deng, MD, PhD
Phone (01186)20-87333300
Email dch0313@163.com
Is FDA regulated No
Health authority China: Ministry of Health
Study type Observational

Clinical Trial Summary

1. Find the early diagnostic markers of erectile dysfunction;

2. Study the warning role of ED in some diseases.


Recruitment information / eligibility

Status Recruiting
Enrollment 150000
Est. completion date January 2020
Est. primary completion date October 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

1. Male and at least 18 years of age.

2. Provide signed informed consent.

3. Have a history of erectile dysfunction (ED: defined as a consistent change in the quality of erection that adversely affects the subject's satisfaction with sexual intercourse) .

4. Have a stable monogamous relationship with a female partner. To some subjects with poor sexual experience, re-evaluation would be conducted after a 4-weeks sex education.

5. Make at least four sexual intercourse attempts with the female sexual study partner during the 4-week therapeutic period without medication.

6. Agree not to use any other ED treatment for at least 4 weeks.

Exclusion Criteria:

1. severe diseases (such as congestive heart failure, arrhythmia, significant renal or hepatic dysfunction and anemia);

2. Had clinically noteworthy penile deformities, pelvic surgery or trauma of perineal region;

3. Had received long-term pharmacotherapy (including antioxidant agents, vitamins and traditional Chinese drugs).

4. An addiction problem (with a history of injection or administration of opium, poppy, heroin, hemp, morphine, cocaine, caffeine, ketamine and meperidine etc.)

Study Design

Observational Model: Case Control


Related Conditions & MeSH terms


Locations

Country Name City State
China The First Affiliated Hospital of Sun Yat-Sen University Guangzhou Guang Dong

Sponsors (2)

Lead Sponsor Collaborator
Sun Yat-sen University Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

Country where clinical trial is conducted

China, 

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