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NCT03008382 · ClinicalTrials.gov registry record · Phase 4
Interstitial Cystitis: Examination of the Central Autonomic Network
A Phase 4 study of Myofascial Pelvic Pain and Interstitial Cystitis/Painful Bladder Syndrome, sponsored by Virginia Commonwealth University.
- Completed
- Registry status
- Phase 4
- Development phase
- 72
- Enrollment target
- 2
- Study locations
NCT03008382 is a Phase 4 study of Myofascial Pelvic Pain and Interstitial Cystitis/Painful Bladder Syndrome that has completed, run by Virginia Commonwealth University. The registered enrollment target is 72 participants. The trial reports 2 study locations across 2 states.
The verdict
NCT03008382, a Phase 4 study of Myofascial Pelvic Pain and Interstitial Cystitis/Painful Bladder Syndrome, has completed, sponsored by Virginia Commonwealth University.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 72 participants
- Enrollment target
- 2
- Study locations
Study Summary
This proposal aims to move the science of chronic pelvic pain (CPP) from simple associations towards an investigation of cause and effect relationships. The investigators will determine whether the striking changes in autonomic nervous system responsiveness (ANS-R) contribute meaningfully to the pathogenesis of CPP.
Conditions Studied
Interventions
- DRUG Placebo Oral Tablet
- DRUG Metoprolol Tartrate Oral Tablet
- OTHER No intervention- observational sub-study
Study Locations (2)
Illinois
- NorthShore University HealthSystem - Evanston
Virginia
- Virginia Commonwealth University - Richmond
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 72 participants |
| Start Date | 2017-03-01 |
| Est. Completion | 2022-03-16 |
| Phase | Phase 4 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03008382
The ClinicalTrials.gov registry entry for NCT03008382 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 72 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Virginia Commonwealth University, which has 558 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Myofascial Pelvic Pain appearing as the primary indexed condition, and to 3 interventions - of which Placebo Oral Tablet is the first listed.
NCT03008382 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Illinois, Virginia.
Frequently Asked Questions
What is clinical trial NCT03008382 about?
NCT03008382 is a clinical study titled "Interstitial Cystitis: Examination of the Central Autonomic Network". This proposal aims to move the science of chronic pelvic pain (CPP) from simple associations towards an investigation of cause and effect relationships. The investigators will determine whether the striking changes in autonomic nervous system responsiveness (ANS-R) contribute meaningfully to the pat...
What is the current status of trial NCT03008382?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 72 participants. The study started on 2017-03-01. Estimated completion is 2022-03-16.
What conditions does trial NCT03008382 study?
This clinical trial studies the following conditions: Myofascial Pelvic Pain, Interstitial Cystitis/Painful Bladder Syndrome.
What interventions are being tested in trial NCT03008382?
The interventions under investigation include: Placebo Oral Tablet (DRUG), Metoprolol Tartrate Oral Tablet (DRUG), No intervention- observational sub-study (OTHER).
Who is sponsoring clinical trial NCT03008382?
This trial is sponsored by Virginia Commonwealth University, which has 558 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03008382 being conducted?
This trial has 2 study locations across Illinois, Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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