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CompletedNCT03148236

Vitamin C in Atrial Fibrillation Ablation

Pilot Study of the Safety and Efficacy of Intravenous Vitamin C in Patients Undergoing Atrial Fibrillation Ablation

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Virginia Commonwealth University · Academic / Other
Sex
All
Age
21 Years
Healthy volunteers
Not accepted

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

Conditions

Interventions

TypeNameDescription
DRUGVitamin C200mg/kg/day split into 4 doses infused every six hours over 30 minutes in 50ml D5W
OTHERPlacebo50mL infused over 30 minutes

Timeline

Start date
2017-09-18
Primary completion
2018-03-13
Completion
2018-03-13
First posted
2017-05-10
Last updated
2019-04-16
Results posted
2019-04-16

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03148236. Inclusion in this directory is not an endorsement.

Vitamin C in Atrial Fibrillation Ablation (NCT03148236) · Clinical Trials Directory