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

This study is enrolling participants by invitation only.

First Received on September 19, 2006. Last Updated on September 30, 2011 History of Changes

Sponsor:	William Beaumont Hospitals
Information provided by (Responsible Party):	William Beaumont Hospitals
ClinicalTrials.gov Identifier:	NCT00379002

Purpose

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

Condition
Interstitial Cystitis Sexual Dysfunction Pelvic Pain

Study Type:	Observational
Study Design:	Time Perspective: Prospective
Official Title:	Comprehensive Database From the WISH (Women's Initiative for Pelvic Pain and Sexual Health) Program in the Department of Urology at Beaumont

Resource links provided by NLM:

MedlinePlus related topics: Interstitial Cystitis Pelvic Pain

U.S. FDA Resources

Further study details as provided by William Beaumont Hospitals:

Estimated Enrollment:	800
Study Start Date:	July 2006
Estimated Study Completion Date:	July 2016

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.

Eligibility

Ages Eligible for Study:	18 Years and older
Genders Eligible for Study:	Female
Accepts Healthy Volunteers:	No
Sampling Method:	Non-Probability Sample

Study Population

All WISH patients

Criteria

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

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00379002

Locations

United States, Michigan
William Beaumont Hospital
Royal Oak, Michigan, United States, 48073

Sponsors and Collaborators

William Beaumont Hospitals

Investigators

Principal Investigator:

Kenneth Peters, M.D.

William Beaumont Hospitals

More Information

No publications provided

Responsible Party:	William Beaumont Hospitals
ClinicalTrials.gov Identifier:	NCT00379002 History of Changes
Other Study ID Numbers:	2006-095
Study First Received:	September 19, 2006
Last Updated:	September 30, 2011
Health Authority:	United States: Institutional Review Board

Keywords provided by William Beaumont Hospitals:

Interstitial Cystitis
Sexual Dysfunction
Vulvodynia
Pelvic Pain

Additional relevant MeSH terms:

Cystitis
Pelvic Pain
Cystitis, Interstitial
Urinary Bladder Diseases

Urologic Diseases
Pain
Signs and Symptoms

ClinicalTrials.gov processed this record on February 12, 2012