- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01830049
Differential Plasma MicroRNA Profiles in ED and Normal Erectile Function in Older Males
April 10, 2013 updated by: Feng Pan, Nanjing Medical University
Erectile dysfunction (ED) is strongly associated with aging.
With the rapidly expanding aging population and the increase in life expectancy, an increase in the prevalence of ED is expected in the years to come.
Currently, the mechanism of ED is not fully understood.
MicroRNAs (MiRNA) are endogenous small RNA molecules that control gene expression post-transcriptionally.
It has been included in many in vitro physiology and pathophysiology processes, which also involved in the process of ED.
This research was designed to investigate the differential plasma MiRNA profiles in ED and normal erectile function in older males.
The results might tell us which MiRNA and how did it involved in the process of ED in aging.
Study Overview
Study Type
Observational
Enrollment (Anticipated)
30
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Jiangsu
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Nanjing, Jiangsu, China, 210000
- Recruiting
- Nanjing Gulou Hospital affiliated to Nanjing University, Medical School
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Contact:
- Yutian Dai, Doctor
- Phone Number: 0086-25-52227777
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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
20 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Sampling Method
Probability Sample
Study Population
Group I: older males came to our clinic for diagnosis and treatment of ED. Group II: older males came to our clinic for physical examination and the erectile function was normal.
Group III: young males came to our clinic for physical examination and the erectile function was normal.
Description
Inclusion Criteria:
- older males with erectile dysfunction
Exclusion Criteria:
- have some other general diseases, e.g. hypertension, vascular diseases, depression, chronic kidney disease, diabetes.
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
- Observational Models: Case-Control
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Group I
Older males with ED
|
|
|
Group II
Older males with normal erectile function
|
|
|
Gourp III
Young males with normal rectile function
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Gene chips
Time Frame: 30 days
|
30 days
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
RT-PCR
Time Frame: 15 days
|
15 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
March 1, 2013
Primary Completion (Anticipated)
July 1, 2013
Study Completion (Anticipated)
August 1, 2013
Study Registration Dates
First Submitted
April 9, 2013
First Submitted That Met QC Criteria
April 10, 2013
First Posted (Estimate)
April 11, 2013
Study Record Updates
Last Update Posted (Estimate)
April 11, 2013
Last Update Submitted That Met QC Criteria
April 10, 2013
Last Verified
April 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NJU2013024
- 2013024 (Other Identifier: Nanjing University, Medical School)
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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