INDEED: Pudendal Assessment in Erectile Dysfunction

Sponsor
University of Pennsylvania (Other)
Overall Status
Terminated
CT.gov ID
NCT01262833
Collaborator
(none)
10
1
36
0.3

Study Details

Study Description

Brief Summary

The study will address the role of internal pudendal artery disease in erectile dysfunction (ED), and whether it might eventually be amenable to intervention with stenting. There is currently a small trial investigating the potential benefit of stenting for erectile dysfunction, but the relationship between pelvic arterial stenoses and erectile dysfunction is not yet proven. The investigators intend to perform angiography on patients both with and without erectile dysfunction, to see whether internal pudendal artery disease is more common in the population with erectile dysfunction. In addition to angiography, stenoses will be examined using fractional flow reserve. The degree of internal pudendal artery disease will then be correlated with the degree of erectile dysfunction using a validated questionnaire, the International Index of Erectile Function (IIEF). Patients will then complete IIEF questionnaires for 5 years to assess the relationship between internal pudendal artery disease and progression of erectile dysfunction.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    10 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    A Cohort Study of the Functional Significance of Internal Pudendal Artery Stenoses in Patients With Erectile Dysfunction
    Study Start Date :
    Sep 1, 2010
    Actual Primary Completion Date :
    Sep 1, 2013
    Actual Study Completion Date :
    Sep 1, 2013

    Arms and Interventions

    Arm Intervention/Treatment
    Cases

    Patients with erectile dysfunction by ILEF questionnaire

    Controls

    Patients without erectile dysfunction by ILEF questionnaire

    Outcome Measures

    Primary Outcome Measures

    1. Pudendal Assessment in Erectile Dysfunction [Up to Five years]

      The primary exposure will be hemodynamically significant internal pudendal artery stenoses as a predictor of erectile dysfunction

    Secondary Outcome Measures

    1. Pudendal Assessment in Erectile Dysfunction [up to five years]

      Secondary analyses will include correlation between bilateral disease and erectile dysfunction, as well as the contribution of small vessel disease (distal to the internal pudendal artery). The severity of disease by IIEF questionnaire will also be compared to the severity of disease by angiography. We will continue through 5-year follow-up of patients with yearly IIEF questionnaires to determine if changes in erectile dysfunction can be predicted by baseline internal pudendal artery disease.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Male
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • As above, men with one risk factor for ED such as age>55, diabetes, hyperlipidemia, smoking, hypertension, coronary disease or peripheral arterial disease
    Exclusion Criteria:
    • Patients with ED from a non-arterial cause, including hormonal, neurological, or trauma-related (as determined by past medical history routinely performed prior to catheterization)

    • Patients requiring urgent catheterization (e.g. acute coronary syndrome or cardiogenic shock)

    • Patients with a creatinine >1.5 mg/dL and those deemed at increased renal risk (such as from receiving >200 mL of dye during the primary procedure, post renal transplant or single kidney), as the additional contrast dye required for angiography would pose an undue risk of progressive kidney disease

    • Patients with other illnesses that reduce their life expectancy to less than one year

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Pennsylvania Philadelphia Pennsylvania United States 19104

    Sponsors and Collaborators

    • University of Pennsylvania

    Investigators

    • Principal Investigator: Howard Herrmann, M.D., University of Pennsylvania

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Pennsylvania
    ClinicalTrials.gov Identifier:
    NCT01262833
    Other Study ID Numbers:
    • 811936
    First Posted:
    Dec 17, 2010
    Last Update Posted:
    Mar 14, 2014
    Last Verified:
    Jan 1, 2012
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 14, 2014