Women's Initiative for Pelvic Pain and Sexual Health (WISH) Program in the Department of Urology at Beaumont - Tabular View

Tracking Information

First Received Date ^ICMJE

September 19, 2006

Last Updated Date

May 4, 2009

Start Date ^ICMJE

July 2006

Primary Completion Date

Current Primary Outcome Measures ^ICMJE

Original Primary Outcome Measures ^ICMJE

Change History

Complete list of historical versions of study NCT00379002 on ClinicalTrials.gov Archive Site

Current Secondary Outcome Measures ^ICMJE

Original Secondary Outcome Measures ^ICMJE

Descriptive Information

Brief Title ^ICMJE

Women's Initiative for Pelvic Pain and Sexual Health (WISH) Program in the Department of Urology at Beaumont

Official Title ^ICMJE

Comprehensive Database From the WISH (Women's Initiative for Pelvic Pain and Sexual Health) Program in the Department of Urology at Beaumont

Brief Summary

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

Detailed 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.

A chart review will be conducted on WISH patient charts.

Study Phase

Study Type ^ICMJE

Observational

Study Design ^ICMJE

Other, Prospective

Condition ^ICMJE

Interstitial Cystitis
Sexual Dysfunction
Pelvic Pain

Intervention ^ICMJE

Study Arms / Comparison Groups

Publications *

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information

Recruitment Status ^ICMJE

Recruiting

Estimated Enrollment ^ICMJE

800

Estimated Completion Date

July 2016

Primary Completion Date

Eligibility Criteria ^ICMJE

Inclusion Criteria:

All 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 WISH program

Gender

Female

Ages

18 Years and older

Accepts Healthy Volunteers

Contacts ^ICMJE

Contact: Donna Carrico, NP

248-551-3565

Location Countries ^ICMJE

United States

Administrative Information

NCT ID ^ICMJE

NCT00379002

Responsible Party

Kenneth Peters, William Beaumont Hospital

Study ID Numbers ^ICMJE

2006-095

Study Sponsor ^ICMJE

William Beaumont Hospitals

Collaborators ^ICMJE

Investigators ^ICMJE

Principal Investigator:

Kenneth Peters, M.D.

William Beaumont Hospitals

Information Provided By

William Beaumont Hospitals

Verification Date

May 2009

^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP