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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00543192
Other study ID # CC07703
Secondary ID H-2007-0204A5328
Status Completed
Phase
First received
Last updated
Start date October 2007
Est. completion date June 2009

Study information

Verified date September 2009
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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


Recruitment information / eligibility

Status Completed
Enrollment 73
Est. completion date June 2009
Est. primary completion date June 2009
Accepts healthy volunteers No
Gender Female
Age group 19 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States University of Wisconsin School of Medicine and Public Health Madison Wisconsin

Sponsors (1)

Lead Sponsor Collaborator
University of Wisconsin, Madison

Country where clinical trial is conducted

United States, 

References & Publications (1)

Onujiogu N, Johnson T, Seo S, Mijal K, Rash J, Seaborne L, Rose S, Kushner DM. Survivors of endometrial cancer: who is at risk for sexual dysfunction? Gynecol Oncol. 2011 Nov;123(2):356-9. doi: 10.1016/j.ygyno.2011.07.035. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Female Sexual Function Index (FSFI). at time of enrollment
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