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NCT01138800 Clinical Trial

Assessing Chronic Pain Conditions in Patients (Pts) With and Without (w&wo) Interstitial Cystitis

Interstitial Cystitis Clinical Trial

Official title:
Assessing Chronic Pain Conditions in Patients With and Without Interstitial Cystitis

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01138800
Other study ID # 2010-094
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 2010
Est. completion date March 2012

Study information
Verified date February 2024
Source William Beaumont Hospitals
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Interstitial cystitis (IC) is a chronic disorder with significant symptoms of urinary urgency, frequency and pelvic pain. IC is more prevalent in women than men. Similar to other chronic pain syndromes such such as irritable bowel syndrome (IBS) and fibromyalgia, the cause of IC is not fully understood. Two subtypes of IC have been identified: classic IC (ulcerative IC) where visible ulcers exist in the bladder and non ulcerative IC, where bladder abnormalities are not apparent but significant bladder-related symptoms exist. We hypothesize that ulcerative IC is a disease of the bladder whereas non ulcerative IC is a more generalized and centrally-mediated chronic pain syndrome similar to IBS and fibromyalgia. To test this hypothesis, we will compare the presence of pain conditions/symptoms in ulcerative vs. non ulcerative IC women vs. community dwelling women (controls) without an IC diagnosis.

Recruitment information / eligibility
Status Completed
Enrollment 666
Est. completion date March 2012
Est. primary completion date March 2012
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Women over 18 years of age with IC identified by investigator (cases); - Women over 18 years of age with IC (controls) Exclusion Criteria: - Male gender; - subjects less than 18 years of age

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States William Beaumont Hospital - Urology Research Royal Oak Michigan

Sponsors (1)
Lead Sponsor Collaborator
William Beaumont Hospitals

Country where clinical trial is conducted

United States, 

See also
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Completed NCT03282318 - A Study to Investigate Efficacy, Safety, Pharmacodynamics and Pharmacokinetics of ASP6294 in the Treatment of Female Subjects With Bladder Pain Syndrome/Interstitial Cystitis Phase 2
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Completed NCT02898220 - Trans-MAPP II Study of Urologic Chronic Pelvin Pain
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Recruiting NCT04845217 - Peppermint Oil for the Treatment of Interstitial Cystitis / Bladder Pain Syndrome Phase 1/Phase 2
Completed NCT04401176 - Bladder Instillations Versus Onabotulinumtoxin A for Treatment of Interstitial Cystitis/Bladder Pain Syndrome Phase 2
Recruiting NCT05147779 - Safety of Cultured Allogeneic Adult Umbilical Cord Stem Cells for Peyronie's Disease, ED, and Interstitial Cystitis Phase 1
Suspended NCT04450316 - Low-dose Naltrexone for Bladder Pain Syndrome Phase 2
Completed NCT04010513 - Hypnosis for Bladder Pain Syndrome N/A
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Completed NCT02232282 - Acupuncture for Female IC/PBSyndrome and Its Effect on the Urinary Microbiome: A Randomized Controlled Trial N/A