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The Women's Urology Center/WISH Database Project

This study is enrolling participants by invitation only.
Information provided by (Responsible Party):
Kenneth Peters, MD, William Beaumont Hospitals Identifier:
First received: September 19, 2006
Last updated: August 26, 2016
Last verified: August 2016
Comprehensive database from the Women's Urology Center/WISH (Women's Initiative for Pelvic Pain and Sexual Health) program at Beaumont.

Interstitial Cystitis
Sexual Dysfunction
Pelvic Pain

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: The Women's Urology Center/WISH Database Project

Further study details as provided by William Beaumont Hospitals:

Estimated Enrollment: 10000
Study Start Date: July 2006
Estimated Study Completion Date: January 2020
Estimated Primary Completion Date: January 2018 (Final data collection date for primary outcome measure)
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.

Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
All Women's Urology Center or WISH patients

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

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT00379002

United States, Michigan
William Beaumont Hospital
Royal Oak, Michigan, United States, 48073
Sponsors and Collaborators
William Beaumont Hospitals
Principal Investigator: Kenneth M Peters, MD William Beaumont Hospital Royal Oak
  More Information

Responsible Party: Kenneth Peters, MD, Principal Investigator, William Beaumont Hospitals Identifier: NCT00379002     History of Changes
Other Study ID Numbers: 2006-095
Study First Received: September 19, 2006
Last Updated: August 26, 2016
Individual Participant Data  
Plan to Share IPD: No

Keywords provided by William Beaumont Hospitals:
Interstitial Cystitis
Sexual Dysfunction
Pelvic Pain

Additional relevant MeSH terms:
Cystitis, Interstitial
Pelvic Pain
Urinary Bladder Diseases
Urologic Diseases
Neurologic Manifestations
Signs and Symptoms processed this record on April 27, 2017