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NCT00379002 Clinical Trial

The Women's Urology Center/WISH Database Project

Sexual Dysfunction Clinical Trial

Official title:
The Women's Urology Center/WISH Database Project

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00379002
Other study ID # 2006-095
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 2006
Est. completion date January 2015

Study information
Verified date March 2020
Source William Beaumont Hospitals
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Comprehensive database from the Women's Urology Center/WISH (Women's Initiative for Pelvic Pain and Sexual Health) program at Beaumont.

Description:

This women's health database will help us to identify health issues/concerns, useful therapies and interventions, and identify areas for improvement or further research specific for women's health. It will allow evaluation of outcomes of clinical interventions to enhance the care and treatment of women with pelvic pain and sexual health concerns.

Recruitment information / eligibility
Status Completed
Enrollment 2923
Est. completion date January 2015
Est. primary completion date January 2015
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

All Women's Urology Center or WISH patients will be included in this database over time.

Exclusion Criteria:

The only exclusion would be if specified by a patient upon consent to treatment in the Women's Urology Center or WISH program

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States William Beaumont Hospital Royal Oak Michigan

Sponsors (1)
Lead Sponsor Collaborator
William Beaumont Hospitals

Country where clinical trial is conducted

United States, 

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