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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, April 2008

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

MedlinePlus related topics:   Interstitial Cystitis   Pelvic Pain  

U.S. FDA Resources

Study Type:   Observational
Study Design:   Other, 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

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 Hospital    
  More Information

Responsible Party:   William Beaumont Hospital ( Kenneth Peters )
Study ID Numbers:   2006-095
First Received:   September 19, 2006
Last Updated:   April 10, 2008
ClinicalTrials.gov Identifier:   NCT00379002
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:
Cystitis, Interstitial
Pelvic Pain
Urinary Bladder Diseases
Cystitis
Pain

Additional relevant MeSH terms:
Signs and Symptoms
Urologic Diseases

ClinicalTrials.gov processed this record on July 03, 2008




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