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Clinical trial

A Phase III Double-Blind, Randomized, Placebo Controlled, Multi-Center Clinical Study to Evaluate the Efficacy and Safety of Intravenous L-citrulline for the Prevention of Clinical Sequelae of Acute Lung Injury Induced by Cardiopulmonary Bypass in Pediatric Subjects Undergoing Surgery for Congenital Heart Defects

NCT02891837 is registered in ClinicalTrials.gov with Asklepion Pharmaceuticals, LLC as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase III Double-Blind, Randomized, Placebo Controlled, Multi-Center Clinical Study to Evaluate the Efficacy and Safety of Intravenous L-citrulline for the Prevention of Clinical Sequelae of Acute Lung Injury Induced by Cardiopulmonary Bypass in Pediatric Subjects Undergoing Surgery for Congenital Heart Defects
Lead sponsor
Asklepion Pharmaceuticals, LLC
Phase
Phase 3
Overall status
Completed
Start date
August 31, 2016
Completion date
July 31, 2019
Enrollment
189 (actual)
Sites
29

Conditions

As the registry lists them; a condition with its own page is linked.