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Linkage Analysis in Interstitial Cystitis

Genetic Studies of Urologic Chronic Pelvic Pain Syndrome

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00675298
Acronym
IC
Enrollment
300
Registered
2008-05-09
Start date
2006-01-31
Completion date
2011-06-30
Last updated
2017-02-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Pelvic Pain Syndrome, Cystitis, Interstitial, Painful Bladder Syndrome, Prostatitis, Urinary Bladder, Overactive

Keywords

Prostatitis, Cystitis, Interstitial, Urinary Bladder, Overactive, Chronic pelvic pain syndrome, Painful bladder syndrome, Urgency, Frequency

Brief summary

Urologic pelvic pain syndrome (UCPPS), variably termed painful bladder syndrome/interstitial cystitis (PBS/IC) in females and chronic prostatitis/chronic pelvic pain syndrome in men (CP/CPPS), is a chronic, debilitating clinical syndrome presenting as severe pelvic pain with extreme urinary urgency and frequency in the absence of any known cause. The etiologic mechanisms underlying UCPPS are unknown, but recurrence, risks to siblings of affected individuals, concordance among monozygotic twins, and our own preliminary studies indicate a strong genetic contribution to the cause of UCPPS. The overall goal of this proposal is use novel approaches to understand the basis of UCPPS, to identify candidate genes containing mutations that result in UCPPS and determine how the different encoded proteins of these genes interact with one another in a common biological pathway. Ultimately, understanding how mutations in at least five different genes yield the symptoms of UCPPS should lead to improved diagnosis and possible therapies.

Interventions

None listed

Sponsors

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH
Beth Israel Deaconess Medical Center
Lead SponsorOTHER

Study design

Observational model
FAMILY_BASED
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
3 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Have symptoms for at least 3 months within the preceding 6 months: * Pain in the pelvic area * Urinary frequency and/or * Urinary urgency and/or * Sexual dysfunction (erectile dysfunction) * Have CP/CPPS, IC, PBS, or BFS * Be willing to provide a saliva and urine sample * Agree to complete several brief questionnaires * Family of someone with CP/CPPS, PBS, IC or BFS * Live in the USA or Canada

Exclusion criteria

* Major structural/anatomical urinary tract abnormalities * Underlying inborn or congenital conditions

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026