The Women's Urology Center/WISH Database Project

This study is enrolling participants by invitation only.
Sponsor:
Collaborator:
William Beaumont Hospitals
Information provided by (Responsible Party):
Donna Carrico, William Beaumont Hospitals
ClinicalTrials.gov Identifier:
NCT00379002
First received: September 19, 2006
Last updated: September 13, 2013
Last verified: September 2013
  Purpose

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


Condition
Interstitial Cystitis
Sexual Dysfunction
Pelvic Pain
Incontinence

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

Resource links provided by NLM:


Further study details as provided by William Beaumont Hospitals:

Estimated Enrollment: 10000
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.

  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 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
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 ClinicalTrials.gov identifier: NCT00379002

Locations
United States, Michigan
William Beaumont Hospital
Royal Oak, Michigan, United States, 48073
Sponsors and Collaborators
Donna Carrico
William Beaumont Hospitals
Investigators
Principal Investigator: Donna Carrico, NP William Beaumont Hospitals
  More Information

No publications provided

Responsible Party: Donna Carrico, Principal Investigator, 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 13, 2013
Health Authority: United States: Institutional Review Board

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

Additional relevant MeSH terms:
Cystitis
Pelvic Pain
Sexual Dysfunctions, Psychological
Cystitis, Interstitial
Urinary Bladder Diseases
Urologic Diseases
Pain
Signs and Symptoms
Sexual and Gender Disorders
Mental Disorders

ClinicalTrials.gov processed this record on July 29, 2014