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Creatine Effect on Brown Adipose Tissue Activation (CreaBAT)

M

Maastricht University

Status

Completed

Conditions

Diet-induced Thermogenesis
Brown Adipose Tissue Activation

Treatments

Dietary Supplement: Creatine monohydrate
Dietary Supplement: placebo cellulose

Study type

Interventional

Funder types

Other

Identifiers

NCT04086381
NL64709.068.18

Details and patient eligibility

About

Pre-clinical studies indicate that creatine may play a substantial role in diet-induced thermogenesis and may have a profound effect on energy balance. A recent retrospective study of BAT activation on PET-CT scans in humans showed a positive association with the estimated renal creatinine clearance and BAT activation, possibly linking creatine metabolism in humans to BAT activity. In humans, so far little options are available to activate brown adipose tissue. The most potent intervention to activate BAT is via cold, which has previously been shown to have metabolic effects in humans. Provided the potential health benefits of brown adipose tissue activation in humans, and provided the role of brown fat in diet induced thermogenesis, we here aim to determine whether creatine monohydrate supplementation can increase diet-induced thermogenesis and activate brown adipose tissue in humans.

Enrollment

14 patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Male or female;
  • 18 to 30 years of age;
  • Consuming a vegetarian diet;
  • BMI 20-25 kg/m2.

Exclusion criteria

  • Not meeting all inclusion criteria;
  • Non-vegetarian diet;
  • Excessive alcohol and/or drug abuse;
  • Significant allergies or intolerances concerning the study products;
  • Participation in another biomedical study within 1 month before the first study visit, possibly interfering with the study results;
  • Medication use known to hamper subject's safety during the study procedures;
  • Subjects with contra-indications for MRI and/or PET-CT;
  • Subjects who do not want to be informed about unexpected medical findings;
  • Subjects who do not want that their treating physician to be informed;
  • Co-morbidities to which the intervention or program that may pose as a complicating factor;
  • Inability to participate and/or complete the required measurements;
  • PET-CT scan in the last 12 months.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

14 participants in 2 patient groups, including a placebo group

Intervention
Active Comparator group
Description:
Oral injestion of 20 grams of creatine monohydrate daily
Treatment:
Dietary Supplement: Creatine monohydrate
Placebo
Placebo Comparator group
Description:
Oral injestion of 20 grams of cellulose daily
Treatment:
Dietary Supplement: placebo cellulose

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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