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Clinical Trial Details — Status: Suspended

Administrative data

NCT number NCT05251207
Other study ID # 2020/39/O/NZ7/01790
Secondary ID
Status Suspended
Phase N/A
First received
Last updated
Start date February 7, 2022
Est. completion date May 31, 2024

Study information

Verified date November 2023
Source Poznan University of Physical Education
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary aims of the current study: - using L-carnitine supplementation modulate the level of plasma trimethylamine N-oxide to assess its effect on circulating cytokines related to diabetes and metabolic syndrome; - using simulated night-shift work intervention as a stress factor, explore the effect of circulating metabolites on insulin sensitivity The secondary aim is to evaluate the effect of carnitine supplementation on gut microbiome composition.


Description:

Subjects will be randomly divided in two groups: supplemented by L-carnitine 2g/day for 12 weeks, and placebo group receiving leucine in identical gelatine capsules. Subjects who successfully complete the protocol will be divided into four subgroups - two with a changed circadian cycle and two controls (supplemented and placebo). Subgroups with a changed daily cycle will be able to sleep between 8:00 and 17:00 for four consecutive days, while during the night they will stay active in the laboratory. The oral glucose tolerance test (OGTT) will be performed before and after the circadian cycle modification. Glucose levels will be monitored by FreeStyle Libre Sensor. Moreover, the activity of the participants will be monitored by wearable activity trackers. Before supplementation, as well as before circadian cycle modification and after finishing the whole experimental procedure, fasting blood samples will be collected for determination of plasma trimethylamine N-oxide (TMAO), trimethylamine (TMA), carnitine (free and acyl derivatives), protein markers of diabetes and inflammation. Moreover, the stool samples will be collected before and after 12 weeks of supplementation, to determine the composition of the gut microbiome. In addition diet of participants will be monitored.


Recruitment information / eligibility

Status Suspended
Enrollment 60
Est. completion date May 31, 2024
Est. primary completion date May 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 30 Years
Eligibility Inclusion Criteria: - healthy volunteers, - must be able to swallow tablets Exclusion Criteria: - smokers, - cardiovascular disease - liver disease - kidney disease - gastrointestinal disorders (including stomach ulcers and erosions) - diabetes

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
L-carnitine
L-carnitine-L-tartrate
L-leucine
L-leucine
Behavioral:
Change of the circadian cycle
Reducing sleep at night for four consecutive days (enabling sleep between 8:00 and 17:00)

Locations

Country Name City State
Poland Akademia Wychowania Fizycznego Poznan

Sponsors (1)

Lead Sponsor Collaborator
Poznan University of Physical Education

Country where clinical trial is conducted

Poland, 

References & Publications (2)

Bescos R, Boden MJ, Jackson ML, Trewin AJ, Marin EC, Levinger I, Garnham A, Hiam DS, Falcao-Tebas F, Conte F, Owens JA, Kennaway DJ, McConell GK. Four days of simulated shift work reduces insulin sensitivity in humans. Acta Physiol (Oxf). 2018 Jun;223(2):e13039. doi: 10.1111/apha.13039. Epub 2018 Feb 12. — View Citation

Samulak JJ, Sawicka AK, Hartmane D, Grinberga S, Pugovics O, Lysiak-Szydlowska W, Olek RA. L-Carnitine Supplementation Increases Trimethylamine-N-Oxide but not Markers of Atherosclerosis in Healthy Aged Women. Ann Nutr Metab. 2019;74(1):11-17. doi: 10.1159/000495037. Epub 2018 Nov 28. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Circulating microbiome metabolites Determination of plasma trimethylamine and trimethylamine N-oxide using ultra performance liquid chromatography - tandem mass spectrometer (UPLC-MS/MS) method 13 weeks
Primary Circulating carnitine metabolites Determination of plasma free, total, and acyl-L-carnitines using ultra performance liquid chromatography - tandem mass spectrometer (UPLC-MS/MS) method 13 weeks
Primary Circulating diabetes biomarkers insulin, C-peptide, ghrelin, leptin, resistin using enzyme-linked immunosorbent assay 13 weeks
Primary Circulating inflammatory biomarkers tumor necrosis factor, C-reactive protein using enzyme-linked immunosorbent assay 13 weeks
Primary Oral Glucose Tolerance Test The subjects will consume 75 g of glucose solution drink within a 5-minute time frame. The glucose level will be continuously monitored with the FreeStyle Libre Sensor. 1 week
Secondary gut microbiome composition 16 S rRNA sequencing will be used to analyze the gut microbiome in the stool samples 13 weeks
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