NCT06344377

Betaine Supplementation and Lipid Metabolism in Overweight and Obese Pre-menopausal Women

The Impact of Betaine Supplementation on Body Composition and Lipid Metabolism in a Group of Overweight and Obese Women
Poznan University of Life Sciences·ClinicalTrials.gov·dietary supplementNot yet recruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Overweight and Obesity
Drug/Device/Intervention
Betaine
Study type
Interventional
Intervention type
dietary supplement
Sponsor & location
Primary sponsor
Poznan University of Life Sciences
Location
Poznań, Poland
Timeline & enrollment
Phase
N/A
Start date
Apr 21, 2024
End date
Dec 30, 2026
Enrollment
60 participants
Primary outcome

Body composition,Body mass,Waist and hips circumference,Lipid profile,Gene expression

Summary

Obesity represents a serious global health issue with significant consequences, including an
 increased risk of chronic diseases. Statistics indicate a growing trend of obesity,
 highlighting the need to seek methods that improve fat tissue metabolism and reduce
 obesity-related complications. Previous research on animals has shown that betaine, a
 substance engaged in one-carbon metabolism, may enhance fat oxidation and lower adipose
 tissue. Therefore, the aim of the research will be to assess the impact of 8-week betaine
 supplementation on body composition and lipid metabolism markers, as well as expression of
 genes related to lipid metabolism, in a group of adult women with abdominal obesity.
 
 This study is designed in a placebo-controlled, double-blinded, randomized fashion. The
 participants will be overweight or obese pre-menopausal females. Upon enrollment,
 participants will be randomly assigned to one of two parallel groups: betaine (3g/d) or
 placebo. The supplementation period will last for 8 weeks. There will be three study
 meetings: T1 before supplementation, T2 after 4 weeks of supplementation, and T3 after 8
 weeks of supplementation. Blood will be drawn and body composition measured, and adipose
 tissue biopsy taken at meetings T1 and T3. The T2 meeting will involve only body composition
 measurement. Study outcomes will include body mass and composition (including body fat
 percent), lipid profile, and the expression of genes related to lipid metabolism in adipose
 tissue and peripheral blood mononuclear cells.

ICD-10 classifications
ObesityOther obesityObesity due to excess caloriesObesity, unspecifiedObesity and other hyperalimentation
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06344377
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06344377 through Pure Global AI's free database. This phase not specified trial is sponsored by Poznan University of Life Sciences and is currently Not yet recruiting. The study focuses on Overweight and Obesity. Target enrollment is 60 participants.

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