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Trial record 85 of 494 for:    penis

Role of Intima-media Thickness in Determining Arteriogenic Erectile Dysfunction

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ClinicalTrials.gov Identifier: NCT03038659
Recruitment Status : Completed
First Posted : February 1, 2017
Last Update Posted : February 1, 2017
Sponsor:
Information provided by (Responsible Party):
Ahmad Raef Sadek, Adam International Hospital

Brief Summary:
Erectile dysfunction.

Condition or disease Intervention/treatment
Erectile Dysfunction Device: Penile Duplex

Detailed Description:
The intima media thickness is increasingly used as a surrogate end point of vascular outcomes in clinical trials aimed at determining the success of interventions that lower risk factors for atherosclerosis and associated diseases (stroke, myocardial infarction and peripheral artery diseases, like disease of cavernosal artery). The investigators hypothesized that the IMT of cavernosal artery would add to the predictive value of vasculogenic erectile dysfunction risk and outcomes. This study seeks to evaluate these hypotheses with our experience, investigating the predictive accuracy of Cavernosal Doppler ultrasound findings for discriminating patients with vasculogenic erectile dysfunction.

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Study Type : Observational
Actual Enrollment : 70 participants
Observational Model: Case-Control
Time Perspective: Prospective
Official Title: Predictive Value of Measuring Intima-media Thickness of Cavernosal Artery in Diagnosis of Arteriogenic Erectile Dysfunction by Penile Duplex
Actual Study Start Date : July 1, 2016
Actual Primary Completion Date : January 1, 2017
Actual Study Completion Date : January 29, 2017

Resource links provided by the National Library of Medicine


Group/Cohort Intervention/treatment
Penile Duplex
Measuring intima media thickness
Device: Penile Duplex
Measuring intima media thickness




Primary Outcome Measures :
  1. erectile dysfunction [ Time Frame: six months ]
    intima media thickness



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 50 Years   (Adult)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
Erectile dysfunction pateints
Criteria

Inclusion Criteria:

  • Erectile dysfunction patients

Exclusion Criteria:

  • Penile trauma.

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Responsible Party: Ahmad Raef Sadek, Dr. Ahmad Raef, Adam International Hospital
ClinicalTrials.gov Identifier: NCT03038659     History of Changes
Other Study ID Numbers: 2018
First Posted: February 1, 2017    Key Record Dates
Last Update Posted: February 1, 2017
Last Verified: January 2017
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Plan Description: Erectile dysfunction

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Erectile Dysfunction
Sexual Dysfunction, Physiological
Genital Diseases, Male
Sexual Dysfunctions, Psychological
Mental Disorders