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Clinical Trial Summary

Single-center, double-blinded, randomized, controlled safety and feasibility pilot study of high dose IV ascorbic acid (200mg/kg) over 24 hours, divided into four doses and administered every six hours with a 30 minute IV infusion time per dose, compared to matched placebo infusion


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03148236
Study type Interventional
Source Virginia Commonwealth University
Contact
Status Completed
Phase Phase 2
Start date September 18, 2017
Completion date March 13, 2018

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