Stopped: Lack of support staff
This is a Phase 2 observational nonrandomized pilot investigation to evaluate the safety and efficacy of Sodium Nitrite administration for the reduction of Primary Graft Dysfunction (PGD) in patients undergoing lung transplant. The study will enroll 8 subjects, undergoing lung transplant at the University of Pittsburgh Medical Center (UPMC).
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Safety of Sodium Nitrite Administration Measured by Methemoglobin Levels
Timeframe: 150 minutes post infusion
Safety of Sodium Nitrite Administration - Number of Participants With Fall in Patient's Mean Arterial Pressure Greater Than 20%
Timeframe: Baseline and 1 hour post infusion