CompletedEarly Phase 1NCT05811377
Phenotyping Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS) by Intravesical Contrast Enhanced - Magnetic Resonance Imaging (ICE-MRI) Bladder Permeability Assay
Studying Interstitial cystitis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Christopher J Chermansky, MD
- Principal Investigator
- Christopher Chermansky, MDUniversity of Pittsburgh
- Intervention
- Ferumoxytol(drug)
- Enrollment
- 8 enrolled
- Eligibility
- 18-80 years · All sexes
- Timeline
- 2023 – 2025
Study locations (1)
- UPMC Magee Women's Hospital, Pittsburgh, Pennsylvania, United States
Collaborators
Lipella Pharmaceuticals, Inc. · National Institutes of Health (NIH)
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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