- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01249703
The Early Diagnosis and Warning Role of Erectile Dysfunction
November 29, 2010 updated by: Sun Yat-sen University
The Early Diagnosis and Warning Role of Erectile Dysfunction:a Multi-institutional Clinical Study.
- Find the early diagnostic markers of erectile dysfunction;
- Study the warning role of ED in some diseases.
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
150000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Chunhua Deng, MD, PhD
- Phone Number: (01186)20-87333300
- Email: dch0313@163.com
Study Contact Backup
- Name: Yanping Huang, MD
- Phone Number: (01186)20-87333300
- Email: hyppin@gmail.com
Study Locations
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Guang Dong
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Guangzhou, Guang Dong, China, 510080
- Recruiting
- The First Affiliated Hospital of Sun Yat-Sen University
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Contact:
- Chunhua Deng, MD, PhD
- Phone Number: (01186) 20-87333300
- Email: dch0313@163.com
-
Contact:
- Yanping Huang, MD
- Phone Number: (01186) 20-87333300
- Email: hyppin@gmail.com
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Principal Investigator:
- Chunhua Deng, MD, PhD
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Sampling Method
Probability Sample
Study Population
men with erectile dysfunction healthy men general male population
Description
Inclusion Criteria:
- Male and at least 18 years of age.
- Provide signed informed consent.
- 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) .
- 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.
- Make at least four sexual intercourse attempts with the female sexual study partner during the 4-week therapeutic period without medication.
- Agree not to use any other ED treatment for at least 4 weeks.
Exclusion Criteria:
- severe diseases (such as congestive heart failure, arrhythmia, significant renal or hepatic dysfunction and anemia);
- Had clinically noteworthy penile deformities, pelvic surgery or trauma of perineal region;
- Had received long-term pharmacotherapy (including antioxidant agents, vitamins and traditional Chinese drugs).
- An addiction problem (with a history of injection or administration of opium, poppy, heroin, hemp, morphine, cocaine, caffeine, ketamine and meperidine etc.)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Chunhua Deng, MD, PhD, Department of Urology
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2008
Primary Completion (Actual)
October 1, 2010
Study Completion (Anticipated)
January 1, 2020
Study Registration Dates
First Submitted
November 29, 2010
First Submitted That Met QC Criteria
November 29, 2010
First Posted (Estimate)
November 30, 2010
Study Record Updates
Last Update Posted (Estimate)
November 30, 2010
Last Update Submitted That Met QC Criteria
November 29, 2010
Last Verified
January 1, 2008
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Chunhua Deng
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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University of BaghdadCompletedSexual Dysfunction | Erectile Dysfunction | Erectile Dysfunction Following Radical Prostatectomy | Erectile Dysfunction Following Radiation Therapy | Sexual Abstinence | Erectile Dysfunction With Diabetes Mellitus | Sexual Desire Disorder | Erectile Dysfunction Following Cryotherapy | Erectile Dysfunction... and other conditionsIraq
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BayerCompletedSexual Dysfunction | Male Erectile DysfunctionBelgium, Italy, France, Germany, Spain, Netherlands, South Africa
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University of VirginiaDIREX SYSTEMS CORPORATIONWithdrawnVasculogenic Erectile Dysfunction
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Johns Hopkins UniversityTerminatedOrganic Erectile DysfunctionUnited States
-
University of MiamiDIREX SYSTEMS CORPORATIONCompletedVasculogenic Erectile DysfunctionUnited States
-
Cairo UniversityCompletedVasculogenic Erectile DysfunctionEgypt
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InitiaTerminatedVasculogenic Erectile DysfunctionIsrael