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NCT01138800 · ClinicalTrials.gov registry record

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

A clinical trial of Interstitial Cystitis, sponsored by Corewell Health East.

Completed
Registry status
666
Enrollment target
1
Study location

NCT01138800 is a study of Interstitial Cystitis that has completed, run by Corewell Health East. The registered enrollment target is 666 participants, above the 337-participant average among 26 other Interstitial Cystitis trials with a reported enrollment target (98% higher). The trial reports 1 study location across 1 state.

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The verdict

NCT01138800, a study of Interstitial Cystitis, has completed, sponsored by Corewell Health East.

COMPLETED
Registry status
666 participants
Enrollment target
1
Study location

Study 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.

Conditions Studied

Study Locations (1)

Michigan

  • William Beaumont Hospital - Urology Research - Royal Oak

Trial Details

FieldValue
Enrollment Target 666 participants
Start Date 2010-05
Est. Completion 2012-03

Sponsor

Corewell Health East

106 total trials

What the Registry Record Tells You About NCT01138800

The ClinicalTrials.gov registry entry for NCT01138800 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 666 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 337-participant average among 26 other Interstitial Cystitis trials with a reported enrollment target (98% higher). The listed sponsor is Corewell Health East, which has 106 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Interstitial Cystitis appearing as the primary indexed condition, and to 0 interventions.

NCT01138800 reports 1 study location spanning 1 distinct geographic area - top geographies include Michigan.

Frequently Asked Questions

What is clinical trial NCT01138800 about?

NCT01138800 is a clinical study titled "Assessing Chronic Pain Conditions in Patients (Pts) With and Without (w&wo) Interstitial Cystitis". 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 underst...

What is the current status of trial NCT01138800?

This trial is currently completed. The enrollment target is 666 participants. The study started on 2010-05. Estimated completion is 2012-03.

What conditions does trial NCT01138800 study?

This clinical trial studies the following conditions: Interstitial Cystitis.

Who is sponsoring clinical trial NCT01138800?

This trial is sponsored by Corewell Health East, which has 106 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01138800 being conducted?

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

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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