Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT02547298 · ClinicalTrials.gov registry record
Interstitial Cystitis (IC)-Like Findings With Hydrodistension
A clinical trial, sponsored by St. Louis University.
- Terminated
- Registry status
- 734
- Enrollment target
NCT02547298: Clinical Trial study, sponsored by St. Louis University.
NCT02547298 is a clinical trial that was terminated before completion, run by St. Louis University. The registered enrollment target is 734 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02547298 was terminated before completion, sponsored by St. Louis University.
- TERMINATED
- Registry status
- 734 participants
- Enrollment target
Study Summary
Patients who are already scheduled to have a gynecologic, urologic or uro-gynecologic procedure involving cystoscopy (a lighted scope is used to look inside the bladder) under anesthesia will be approached to participate in the study. Once prospective study subjects are consented, they will be requested to complete the study questionnaires. At the time of the procedure, during the cystoscopy, patients will undergo hydrodistension (stretching the bladder with fluid). Photographic images of the bladder will be collected, to be later analyzed by examiners. Patients who have positive findings for interstitial cystitis during cystoscopy with hydrodistension, will be notified of the findings after the procedure. They will be asked to fill out an additional, previously completed questionnaire at the time of a follow-up visit, during a phone interview or responding to the questionnaire via a secure web site. These patients will be treated for interstitial cystitis by their primary providers as clinically indicated.
Primary Outcome
Change From Baseline in Pain on the 11 point Short Pain Scale (SPS-11).
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 734 participants |
| Start Date | 2015-06 |
| Est. Completion | 2018-01-18 |
Why NCT02547298 stopped before completion
NCT02547298 is an observational study that tracks outcomes without assigning an intervention. The registered 734 participants enrollment target is mid-sized for trials with a published cap.
The record links to 0 conditions, and to 0 interventions.
NCT02547298 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02547298 about?
NCT02547298 is a clinical study titled "Interstitial Cystitis (IC)-Like Findings With Hydrodistension". Patients who are already scheduled to have a gynecologic, urologic or uro-gynecologic procedure involving cystoscopy (a lighted scope is used to look inside the bladder) under anesthesia will be approached to participate in the study. Once prospective study subjects are consented, they will be reque...
What is the current status of trial NCT02547298?
This trial is currently terminated. The enrollment target is 734 participants. The study started on 2015-06. Estimated completion is 2018-01-18.
Who is sponsoring clinical trial NCT02547298?
This trial is sponsored by St. Louis University, which has 107 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT06216301 · 734 participants · Phase 3
LUNAR-2: TTFields With Pembrolizumab + Platinum-based Chemotherapy for Metastatic NSCLC
- NCT07231419 · 734 participants · Phase 3
Evaluation of Efficacy and Safety of Suzetrigine (SUZ) for Pain Associated With Diabetic Peripheral Neuropathy
- NCT05947851 · 735 participants · Phase 3
A Study of Nemtabrutinib Plus Venetoclax vs Venetoclax + Rituximab (VR) in Second-line (2L) + Relapsed/Refractory (R/R) Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma (CLL/SLL) (MK-1026-010/BELLWAVE-010).
- NCT05999084 · 735 participants
Georgia Memory Net Anti-Amyloid Monoclonal Antibody Registry
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia