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Effects of Carnipure® Tartrate on Postprandial Endothelial Function and Recovery

NCT02635594 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2016-09-07

No results posted yet for this study

Summary

Investigation of 4 weeks supplementation with Carnipure® tartrate on endothelial function and parameters of recovery after physical exertion.

Conditions

  • Healthy Volunteers
  • Recovery
  • Endothelial Function

Interventions

DIETARY_SUPPLEMENT

L-Carnitine

1000mg of L-Carnitine provided as 1475mg Carnipure® tartrate

OTHER

Placebo

1000mg cellulose + 475mg L-tartaric acid

Sponsors & Collaborators

  • Lonza Ltd.

    lead INDUSTRY

Principal Investigators

  • Daniel Menzel, PhD · BioTeSys GmbH

Study Design

Allocation
RANDOMIZED
Masking
QUADRUPLE
Model
CROSSOVER

Eligibility

Min Age
25 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-12-31
Primary Completion
2016-06-30
Completion
2016-06-30

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02635594 on ClinicalTrials.gov