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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00550121
Other study ID # CHFVIT
Secondary ID
Status Completed
Phase N/A
First received October 25, 2007
Last updated October 13, 2008
Start date August 2007
Est. completion date April 2008

Study information

Verified date October 2008
Source Radboud University
Contact n/a
Is FDA regulated No
Health authority Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)
Study type Interventional

Clinical Trial Summary

In CHF central sympathetic activity is increased. ROS formation seems to play a role in this process. This study analyzes the effect of vitamin C as an antioxidant on central sympathetic activity in CHF


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date April 2008
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- Heart failure of at least New York Heart Association (NYHA) class II

- Left ventricular ejection fraction (LVEF) <= 40%

- Age 20-80 years

Exclusion Criteria:

- Necessity of short-term PCI, CABG or heart transplantation,

- Chronic disease of the autonomic nervous system,

- diabetes mellitus,

- use of tricyclic antidepressant drugs and/or a-adrenergic receptor antagonists.

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator)


Related Conditions & MeSH terms


Intervention

Drug:
vitamin C

placebo


Locations

Country Name City State
Netherlands Radboud University Nijmegen Medical Centre Nijmegen

Sponsors (2)

Lead Sponsor Collaborator
Radboud University ZonMw: The Netherlands Organisation for Health Research and Development

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary change in central sympathetic output after vitamin C vs. placebo
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