CompletedPhase 1NCT01150565
Safety Study of LiRIS in Interstitial Cystitis (IC) Patients
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
- Allergan
- Principal Investigator
- Curtis Nickel, MD, MSN NPQueen's University/Kingston General Hospital
- Intervention
- LiRIS low dose and LiRIS high dose(drug)
- Enrollment
- 18 enrolled
- Eligibility
- 18 years · FEMALE
- Timeline
- 2010 – 2011
Study locations (3)
- Dr. Steinhoff Clinical Research, Victoria, British Columbia, Canada
- Queen Elizabeth II Health Sciences Centre, Halifax Infirmary, Halifax, Nova Scotia, Canada
- Centre for Applied Urological Research, Kingston, Ontario, Canada
Collaborators
TARIS Biomedical, Inc.
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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