drugset / Trial / NCT03148236

Vitamin C in Atrial Fibrillation Ablation

NCT03148236

Phase 2 Completed 20 enrolled Virginia Commonwealth University
RandomizedParallel-groupQuadruple-blindTreatment

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

Timeline

Start
2017-09-18
Primary completion
2018-03-13
Completion
2018-03-13

Drugs

EvaluationDrugModalityDoseRoute
Comparator Vitamin C Other / unclassified 200 mg/kg Intravenous

Indications