NCT00817388

Brief Summary

Completion of a brief survey tool and providing an urine specimen. The study purpose is to improve our understanding of interstitial cystitis and painful pelvic syndrome.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
26

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Jan 2009

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2009

Completed
4 days until next milestone

First Submitted

Initial submission to the registry

January 5, 2009

Completed
1 day until next milestone

First Posted

Study publicly available on registry

January 6, 2009

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2010

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2010

Completed
Last Updated

June 7, 2010

Status Verified

June 1, 2010

Enrollment Period

1.3 years

First QC Date

January 5, 2009

Last Update Submit

June 4, 2010

Conditions

Interstitial CystitisPelvic Pain

Keywords

Interstitial cystitispelvic pain

Outcome Measures

Primary Outcomes (1)

  • To correlate IC/PBS symptoms with urine biomarkers

    2 years

Study Arms (1)

1

patients will be asked to provide a urine specimen and complete a questionnaire.

Other: No intervention

Interventions

No interventionOTHER

No intervention

1

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with and without intersitial cystitis/painful pelvic pain will be asked to provide an urine specimen and complete a brief questionnaire.

You may qualify if:

  • Men and women with interstitial cystitis/painful bladder syndrome greater than 18 years old
  • Male and female controls without a history of IC/PBS diagnosis

You may not qualify if:

  • \. Unable to complete questionnaires and/or give informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

William Beaumont Hospital

Royal Oak, Michigan, 48073, United States

Location

Biospecimen

Retention: SAMPLES WITHOUT DNA

Urine specimen.

MeSH Terms

Conditions

Cystitis, InterstitialPelvic Pain

Condition Hierarchy (Ancestors)

CystitisUrinary Bladder DiseasesUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Michael Chancellor, MD

    Corewell Health East

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Sponsor Type
OTHER

Study Record Dates

First Submitted

January 5, 2009

First Posted

January 6, 2009

Study Start

January 1, 2009

Primary Completion

May 1, 2010

Study Completion

May 1, 2010

Last Updated

June 7, 2010

Record last verified: 2010-06

Locations

US(1)