Status:
COMPLETED
Relationship: Interstitial Cystitis & Vulvodynia-Part 2
Lead Sponsor:
Corewell Health East
Conditions:
Vulvodynia
Eligibility:
FEMALE
18+ years
Brief Summary
The etiology of pain in women with IC is often difficult to identify resulting in unnecessary medical and surgical treatments (e.g. hysterectomies). The vulva may actually be the site of some of the r...
Detailed Description
In a mailed survey (Part 1 of this study), 127 women with a documented diagnosis of IC agreed to be contacted for an in-office examination. The mailed survey was internally developed specifically for ...
Eligibility Criteria
Inclusion
- Inclusion Criteria
- Women with interstitial cystitis and vulvar pain who agreed to be contacted in Part 1 (HIC #2007-183) of this study.
- Age 18 or older
- Capable of giving informed consent
- Capable and willing to follow all study procedures
- Exclusion Criteria:
- Pregnant women· Vaginitis (may be treated, then tested later)
- Vulvar disease (other than vulvodynia)-lichen planus, lichen sclerosis, neoplasia
- The subject is deemed unsuitable for enrollment by the investigators based on their history or physical examination.
- Neuropathy
Exclusion
Key Trial Info
Start Date :
September 1 2008
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
September 1 2008
Estimated Enrollment :
127 Patients enrolled
Trial Details
Trial ID
NCT00751010
Start Date
September 1 2008
End Date
September 1 2008
Last Update
October 15 2008
Active Locations (1)
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1
William Beaumont Hospital
Royal Oak, Michigan, United States, 48073