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Vitamin C Supplementation Intervention for Patients With Heart Failure-A Pilot Study
This study is to test a low-cost, simple vitamin C supplementation intervention, that is, comparing placebo to 500 mg/day vitamin C and 1 gram/day vitamin C daily to assess feasibility and acceptability of vitamin C supplementation and effects on serum vitamin C level, health-related quality of life (HRQOL), symptom burden, oxidative stress, and cardiac function.
This study will address feasibility from the perspective of being able to: a) to detect significant differences in the serum vitamin C level after supplementation (3 months) between the intervention groups and the control group, b) to detect significant differences in health related quality of life (HRQOL), symptom burden, oxidative stress, and cardiac function after vitamin C supplementation (3 months) between the intervention groups and the control group.
Age
18 - 99 years
Sex
ALL
Healthy Volunteers
No
UNCH Meadowmont Clinic
Chapel Hill, North Carolina, United States
Start Date
August 14, 2018
Primary Completion Date
June 16, 2020
Completion Date
June 16, 2020
Last Updated
March 9, 2021
36
ACTUAL participants
Vitamin C 500 mg
DIETARY_SUPPLEMENT
Vitamin C 1000 mg
DIETARY_SUPPLEMENT
Placebo
OTHER
Lead Sponsor
University of North Carolina, Chapel Hill
Collaborators
NCT07191730
NCT07484009
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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