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OpenTrials
Completed

NCT Number: NCT01303848

Circadian Rhythm of Blood Lactate

To elucidate whether blood lactate, lipid transfer proteins and PPARs/CLOCK/Bal1 have a circadian rhythm

Completed

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Key information

Conditions

Healthy

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Observational

Primary location

University Clinic Halle, Martin Luther-University Halle-Wittenberg

Halle, 06120, Germany

About this study

Blood will be drawn fasting and then every hour over a period of 24 hours in 30 healthy probands.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Age between 18 and 40 years old

Exclusion criteria

  • Inability/unwilling to give written informed consent
  • Chronic disease

Treatment and study plan

Blood sampling

Other

Blood Sampling over 24 hours

Primary outcomes

  1. Circadian rhythm of blood lactate

    Time frame: 5 months

    Blood samples

Secondary outcomes

  1. Circadian rhythm of Lipid transfer proteins

    Time frame: 5 months

    Blood

  2. Circadian rhythm of PPARs, CLOCK and Bal1

    Time frame: 5 months

    Blood

Sponsors and collaborators

Lead sponsor

Martin-Luther-Universität Halle-Wittenberg

Other

Collaborators

  • State University of New York - Downstate Medical Center

Registry information

Official study title

Circadian Rhythm of Blood Lactate, Lipid Transferproteins and Genetic Markers (PPARs, CLOCK, Bmal1)

Important dates

Study start
2011
Primary completion
2011
Study completion
2012
First posted
Feb 25, 2011
Registry last updated
May 2, 2012

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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