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NCT00675298 · ClinicalTrials.gov registry record

Linkage Analysis in Interstitial Cystitis

A clinical trial of Chronic Pelvic Pain Syndrome and Urinary Bladder, Overactive, sponsored by Beth Israel Deaconess Medical Center.

Completed
Registry status
300
Enrollment target
1
Study location

NCT00675298: Completed study of Chronic Pelvic Pain Syndrome and Urinary Bladder, Overactive, sponsored by Beth Israel Deaconess Medical Center.

NCT00675298 is a study of Chronic Pelvic Pain Syndrome and Urinary Bladder, Overactive that has completed, run by Beth Israel Deaconess Medical Center. The registered enrollment target is 300 participants, above the 169-participant average among 11 other Chronic Pelvic Pain Syndrome trials with a reported enrollment target (78% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00675298, a study of Chronic Pelvic Pain Syndrome and Urinary Bladder, Overactive, has completed, sponsored by Beth Israel Deaconess Medical Center.

COMPLETED
Registry status
300 participants
Enrollment target
1
Study location

Study 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.

Study Locations (1)

Massachusetts

  • Jordan D Dimitrakoff - Boston

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 2006-01
Est. Completion 2011-06

What the finished NCT00675298 record still lists

NCT00675298 is an observational study that tracks outcomes without assigning an intervention. The registered 300 participants enrollment target is mid-sized for trials with a published cap, above the 169-participant average among 11 other Chronic Pelvic Pain Syndrome trials with a reported enrollment target (78% higher).

The record links to 5 conditions, with Chronic Pelvic Pain Syndrome appearing as the primary indexed condition, and to 0 interventions.

NCT00675298 reports a single indexed study location in Massachusetts.

Frequently Asked Questions

What is clinical trial NCT00675298 about?

NCT00675298 is a clinical study titled "Linkage Analysis in Interstitial Cystitis". 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 ...

What is the current status of trial NCT00675298?

This trial is currently completed. The enrollment target is 300 participants. The study started on 2006-01. Estimated completion is 2011-06.

What conditions does trial NCT00675298 study?

This clinical trial studies the following conditions: Chronic Pelvic Pain Syndrome, Urinary Bladder, Overactive, Painful Bladder Syndrome, Cystitis, Interstitial, Prostatitis.

Who is sponsoring clinical trial NCT00675298?

This trial is sponsored by Beth Israel Deaconess Medical Center, which has 488 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00675298 being conducted?

This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Chronic Pelvic Pain Syndrome

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00675298's enrollment target sits among peer trials

300 2nd of 11 the highest of 11 other Chronic Pelvic Pain Syndrome trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Chronic Pelvic Pain Syndrome trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00675298, the US trial registry maintained by the National Library of Medicine. NCT00675298 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.