TerminatedNot applicableNCT02517996
Use of Preemptive Pudendal Nerve Block Prior to Hydrodistention for the Treatment of Interstitial Cystitis/Painful Bladder Syndrome (IC/PBS)
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
- Johns Hopkins University
- Principal Investigator
- Tola Fashokun, M.D.Johns Hopkins University
- Intervention
- Lidocaine(drug)
- Enrollment
- 18 enrolled
- Eligibility
- 18 years · FEMALE
- Timeline
- 2015 – 2018
Study locations (2)
- Greater Baltimore Medical Center, Baltimore, Maryland, United States
- Johns Hopkins Bayview Medical Center, Baltimore, Maryland, United States
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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