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

This study is currently recruiting participants.

Verified by William Beaumont Hospitals, May 2009

First Received: September 19, 2006 Last Updated: May 4, 2009 History of Changes

Sponsored by:	William Beaumont Hospitals
Information provided by:	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:	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:

Biospecimen Retention: None Retained

Biospecimen Description:

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

Contacts

Contact: Donna Carrico, NP

248-551-3565

Locations

United States, Michigan
William Beaumont Hospital	Recruiting
Royal Oak, Michigan, United States, 48073
Contact: Donna Carrico, NP 248-551-3565
Sub-Investigator: Carrico Donna, NP

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 Hospital ( Kenneth Peters )
Study ID Numbers:	2006-095
Study First Received:	September 19, 2006
Last Updated:	May 4, 2009
ClinicalTrials.gov Identifier:	NCT00379002 History of Changes
Health Authority:	United States: Institutional Review Board

Keywords provided by William Beaumont Hospitals:

Interstitial Cystitis
Sexual Dysfunction
Vulvodynia
Pelvic Pain

Study placed in the following topic categories:

Signs and Symptoms
Cystitis, Interstitial
Cystocele
Pelvic Pain

Urologic Diseases
Urinary Bladder Diseases
Cystitis
Pain

Additional relevant MeSH terms:

Signs and Symptoms
Cystitis, Interstitial
Pelvic Pain
Urologic Diseases

Urinary Bladder Diseases
Cystitis
Pain

ClinicalTrials.gov processed this record on July 06, 2009