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OpenTrials
Completed

NCT Number: NCT02535897

Protein Ingestion and Muscle Carnitine Uptake

The purpose of this study is to assess the effects of a protein-carbohydrate beverage on the absorption of an orally ingested bolus of L-carnitine, compared to flavoured water and carbohydrate-only controls, and to determine whether increasing plasma carnitine availability can impact upon insulin-stimulated muscle carnitine uptake.

Completed

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Key information

Conditions

Age range

18 year–35 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy
  • Body mass index of 18-25 kg/cm2

Exclusion criteria

  • Unhealthy
  • Smoker
  • Taking any medication that interferes with skeletal muscle metabolism

Treatment and study plan

Flavoured water

Dietary Supplement

Flavoured water + carbohydrate

Dietary Supplement

Flavoured water + carbohydrate + protein

Dietary Supplement

Primary outcomes

  1. Muscle carnitine uptake

    Time frame: 180 minutes

    Change in forearm carnitine uptake (measured using arterialised-venous - venous balance technique) in response to intervention.

Sponsors and collaborators

Lead sponsor

University of Nottingham

Other

Registry information

Official study title

The Effects of an Insulinotropic Protein-carbohydrate Beverage on L- Carnitine Absorption and Muscle Carnitine Uptake

Important dates

Study start
2013
Primary completion
2014
Study completion
2014
First posted
Aug 31, 2015
Registry last updated
Aug 31, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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