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The Women's Urology Center/WISH Database Project

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ClinicalTrials.gov Identifier: NCT00379002
Recruitment Status : Enrolling by invitation
First Posted : September 21, 2006
Last Update Posted : December 25, 2017
Sponsor:
Information provided by (Responsible Party):

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

Condition or disease
Interstitial Cystitis Sexual Dysfunction Pelvic Pain Incontinence

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.

Study Design

Study Type : Observational
Estimated Enrollment : 10000 participants
Observational Model: Other
Time Perspective: Prospective
Official Title: The Women's Urology Center/WISH Database Project
Actual Study Start Date : July 2006
Estimated Primary Completion Date : January 2019
Estimated Study Completion Date : January 2020
Groups and Cohorts


Outcome Measures

Eligibility Criteria

Information from the National Library of Medicine

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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
Criteria

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00379002


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

Responsible Party: Kenneth Peters, MD, Principal Investigator, William Beaumont Hospitals
ClinicalTrials.gov Identifier: NCT00379002     History of Changes
Other Study ID Numbers: 2006-095
First Posted: September 21, 2006    Key Record Dates
Last Update Posted: December 25, 2017
Last Verified: December 2017
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Keywords provided by Kenneth Peters, MD, William Beaumont Hospitals:
Interstitial Cystitis
Sexual Dysfunction
Vulvodynia
Pelvic Pain
incontinence

Additional relevant MeSH terms:
Pelvic Pain
Cystitis
Cystitis, Interstitial
Pain
Neurologic Manifestations
Signs and Symptoms
Urinary Bladder Diseases
Urologic Diseases