Condition: Ureter Injury · Sponsor: Prove pharm
This is an open label, randomized, multicenter study to evaluate the efficacy and safety of two dose levels (2.5 mL and 5.0 mL) of Indigotindisulfonate Sodium Injection, USP 0.8% when used as an aid in the determination of ureteral patency in patients with different degrees of renal impairment.
This description comes directly from the study's public registry record.
Michelle Boytim, P.hD. · 610-850-7115 · michelle.boytim@provepharm.com
Always discuss trial participation with your own doctor first.
| Albany Medical Center | Albany, New York, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06085183