Circadian Rhythm of Blood Lactate
This study has been completed.
Sponsor:
Martin-Luther-Universität Halle-Wittenberg
Collaborator:
State University of New York - Downstate Medical Center
Information provided by (Responsible Party):
Axel Schlitt, Martin-Luther-Universität Halle-Wittenberg
ClinicalTrials.gov Identifier:
NCT01303848
First received: February 24, 2011
Last updated: May 1, 2012
Last verified: May 2012
| Tracking Information | |||||
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| First Received Date ICMJE | February 24, 2011 | ||||
| Last Updated Date | May 1, 2012 | ||||
| Start Date ICMJE | February 2011 | ||||
| Primary Completion Date | December 2011 (final data collection date for primary outcome measure) | ||||
| Current Primary Outcome Measures ICMJE |
Circadian rhythm of blood lactate [ Time Frame: 5 months ] [ Designated as safety issue: No ] Blood samples |
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| Original Primary Outcome Measures ICMJE | Same as current | ||||
| Change History | Complete list of historical versions of study NCT01303848 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE |
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| Original Secondary Outcome Measures ICMJE | Same as current | ||||
| Current Other Outcome Measures ICMJE | Not Provided | ||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||
| Descriptive Information | |||||
| Brief Title ICMJE | Circadian Rhythm of Blood Lactate | ||||
| Official Title ICMJE | Circadian Rhythm of Blood Lactate, Lipid Transferproteins and Genetic Markers (PPARs, CLOCK, Bmal1) | ||||
| Brief Summary | To elucidate whether blood lactate, lipid transfer proteins and PPARs/CLOCK/Bal1 have a circadian rhythm |
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| Detailed Description | Blood will be drawn fasting and then every hour over a period of 24 hours in 30 healthy probands. |
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| Study Type ICMJE | Observational | ||||
| Study Design ICMJE | Time Perspective: Prospective | ||||
| Target Follow-Up Duration | Not Provided | ||||
| Biospecimen | Not Provided | ||||
| Sampling Method | Non-Probability Sample | ||||
| Study Population | 30 healthy probands |
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| Condition ICMJE | Healthy | ||||
| Intervention ICMJE | Other: Blood Sampling
Blood Sampling over 24 hours |
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| Study Group/Cohort (s) | Healthy probands
Healthy probands, age between 18 and 40 years
Intervention: Other: Blood Sampling |
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| Publications * | Not Provided | ||||
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status ICMJE | Completed | ||||
| Enrollment ICMJE | 30 | ||||
| Completion Date | May 2012 | ||||
| Primary Completion Date | December 2011 (final data collection date for primary outcome measure) | ||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||
| Ages | 18 Years to 40 Years | ||||
| Accepts Healthy Volunteers | Yes | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | Germany | ||||
| Administrative Information | |||||
| NCT Number ICMJE | NCT01303848 | ||||
| Other Study ID Numbers ICMJE | UKH2011Sport1 | ||||
| Has Data Monitoring Committee | No | ||||
| Responsible Party | Axel Schlitt, Martin-Luther-Universität Halle-Wittenberg | ||||
| Study Sponsor ICMJE | Martin-Luther-Universität Halle-Wittenberg | ||||
| Collaborators ICMJE | State University of New York - Downstate Medical Center | ||||
| Investigators ICMJE |
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| Information Provided By | Martin-Luther-Universität Halle-Wittenberg | ||||
| Verification Date | May 2012 | ||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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