Sexual Functioning in Endometrial Cancer

Sponsor
University of Wisconsin, Madison (Other)
Overall Status
Completed
CT.gov ID
NCT00543192
Collaborator
(none)
73
1
20
3.6

Study Details

Study Description

Brief Summary

The purpose of this study is estimate how sexual function in endometrial cancer survivors varies with severity of disease.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    73 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Cross-Sectional
    Official Title:
    Sexual Functioning in Endometrial Cancer Survivors
    Study Start Date :
    Oct 1, 2007
    Actual Primary Completion Date :
    Jun 1, 2009
    Actual Study Completion Date :
    Jun 1, 2009

    Outcome Measures

    Primary Outcome Measures

    1. Female Sexual Function Index (FSFI). [at time of enrollment]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    19 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • History of Stage I-IIIA endometrial adenocarcinoma of any grade

    • 1-5 years out from primary surgical treatment

    • Adjuvant therapy may only have consisted of radiation or hormonal therapy

    • No evidence of disease

    Exclusion Criteria:
    • Previous treatment for other malignancies

    • Did not undergo surgery for primary treatment of endometrial cancer

    • Inability to read, write and speak fluent English

    • Major cognitive impairment affecting ability to provide consent

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Wisconsin School of Medicine and Public Health Madison Wisconsin United States 53792

    Sponsors and Collaborators

    • University of Wisconsin, Madison

    Investigators

    • Principal Investigator: David M Kushner, MD, University of Wisconsin, Madison

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    University of Wisconsin, Madison
    ClinicalTrials.gov Identifier:
    NCT00543192
    Other Study ID Numbers:
    • CC07703
    • H-2007-0204
    • A532820
    • SMPH/OBSTET & GYNECOL
    First Posted:
    Oct 12, 2007
    Last Update Posted:
    Nov 19, 2019
    Last Verified:
    Sep 1, 2009
    Keywords provided by University of Wisconsin, Madison
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 19, 2019