Clinical Trials Logo

Clinical Trial Details — Status: Suspended

Administrative data

NCT number NCT04651205
Other study ID # 200180160
Secondary ID
Status Suspended
Phase N/A
First received
Last updated
Start date October 2021
Est. completion date October 2022

Study information

Verified date April 2021
Source University of Glasgow
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Magnesium (Mg) and thiamine (vitamin B1) are micronutrients involved in the regulation of blood sugar level. Avoidance of wholegrains or fruits and starchy vegetables could impact on Mg and vitamin B1 intakes and status. Although supplementation can be recommended alongside low-carbohydrate high fat diets (LCHF) diets, its benefits have never been studied before. This study aims to test the effect of Mg and vitamin B1 supplements on glucose metabolism in people following any LCHF diet.


Description:

It is clear that Mg involves in both type 2 diabetes (T2D) prevention and management, and following LCHF diets, avoidance of wholegrains, fruits and starchy vegetables, could have a negative impact on Mg and B1 intakes and status. A systematic review of LCHF diets and micronutrients confirmed that Mg and B1 intakes were reduced by 50% and 70% following LCHF diets compared to baseline normal carbohydrate diets, and could be as low as 40% and 75% of recommended intakes for Mg and B1 respectively. Although supplementation can be recommended alongside LCHF diets, not all LCHF dieters take supplements, and their benefits during LCHF diets have never been studied before. Rationale We hypothesise that people who have been following LCHF diets without taking supplement are potentially at risk of Mg/B1 insufficiency, with negative impact on glucose metabolism. Objective 1. To investigate potential efficacy of Mg/B1 supplementation on glucose metabolism (mechanistic efficacy/proof of concept) in adults already voluntarily following LCHF 2. To investigate effect of Mg/B1 supplementation on Mg/B1 status in adults already voluntarily following LCHF, who are at risk of Mg/B1 inadequacy 3. To test capabilities of measures, procedures, recruitment criteria, and operational strategies that are under consideration for use in a subsequent, larger, study. 4. To identify barriers to successful study completion 5. To evaluate acceptability of methods and instruments to participants Study design: This is a mechanistic efficacy/proof of concept, intervention study with a use of a randomised-start design. All participants will be assigned to the same intervention but at different times. There are 3 groups of the study - 2 interventions and 1 control group: 1. 400 mg of Mg per day for 4 weeks then add on 100 mg of B1 per day for another 4 weeks, a total duration of 8 weeks (MB). 2. 100 mg of B1 per day for 4 weeks then add on 400 mg of Mg per day for another 4 weeks, a total duration of 8 weeks (BM). 3. Untreated: Participants with delayed entry (untreated) for 8 weeks (Con) Assessment: Baseline, 4 weeks, and 8 weeks after intervention/untreated period


Recruitment information / eligibility

Status Suspended
Enrollment 18
Est. completion date October 2022
Est. primary completion date October 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. aged 18 years and older 2. have been following LCHF diets for at least 2 months 3. carbohydrate intake is less than 130 g/day or less than 26% of energy intake 4. have stable body weight (weight change = 2 kg within two months period) 5. no diagnosed or suspected eating disorder. Exclusion Criteria: 1. currently taking Mg and B1 supplements within the last 3 months 2. underweight defined by BMI below 18.5 kg/m2 3. have been diagnosed with T1DM or other types of diabetes apart from T2DM. 4. if potential participants have been diagnosed with T2DM, they will be excluded if they are on anti-diabetic drugs and/or insulin (see 7.) or if they are currently following a complete diet for weight loss (e.g. meal replacement, Slimfast, etc.) 5. currently taking anti-diabetic drugs (e.g. metformin, sulfonylurea, GLP-1 agonist, DPP4-inhibitor, SGLT-2 inhibitor, etc) nor insulin use 6. currently taking medications that interact with Mg supplement 7. currently taking medications that may affect glucose metabolism such as steroids, hormonal therapy (e.g. hormone replacement therapy in postmenopausal), antipsychotics. 8. pregnant and lactating women. 9. have gastrointestinal tract diseases e.g. Inflammatory bowel diseases, irritable bowel syndrome, coeliac disease, including other diseases that involve malabsorption. 10. have kidney disease or impair renal function 11. have auto-immune/connective tissue diseases, malignancy. 12. currently dieting or losing 5% of body weight or more during the last 6 months (or planning to do so in the following year). 13. currently participating in other intervention studies.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
vitamin B1 and magnesium supplements
vitamin B1 - 100 mg/day magnesium - 400 mg/day

Locations

Country Name City State
United Kingdom University of Glasgow Glasgow

Sponsors (1)

Lead Sponsor Collaborator
University of Glasgow

Country where clinical trial is conducted

United Kingdom, 

References & Publications (1)

Churuangsuk C, Griffiths D, Lean MEJ, Combet E. Impacts of carbohydrate-restricted diets on micronutrient intakes and status: A systematic review. Obes Rev. 2019 Aug;20(8):1132-1147. doi: 10.1111/obr.12857. Epub 2019 Apr 22. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary fasting plasma glucose changes from baseline and after supplementation 8 weeks
Primary fasting insulin changes from baseline and after supplementation 8 weeks
Primary homeostatic model assessment of insulin resistance (HOMA-IR) changes from baseline and after supplementation 8 weeks
Primary incremental area under the curve (iAUC) of glucose and insulin after 75 g oral glucose tolerance test changes from baseline and after supplementation 8 weeks
Primary magnesium status changes from baseline and after supplementation 8 weeks
Primary vitamin B1 status changes from baseline and after supplementation 8 weeks
Secondary lipid profile: plasma Triglyceride, Total cholesterol, LDL-cholesterol, HDL-cholesterol changes from baseline and after supplementation 8 weeks
Secondary plasma hs-CRP changes from baseline and after supplementation 8 weeks
Secondary plasma IL-6 changes from baseline and after supplementation 8 weeks
Secondary sRAGE changes from baseline and after supplementation 8 weeks
Secondary Urine 8-isoprostane , MDA, glycation markers (fructosamine and HbA1c, dermal glycation by skin fluorescence) 8 weeks
Secondary plasma 8-isoprostane changes from baseline and after supplementation 8 weeks
Secondary plasma fructosamine changes from baseline and after supplementation 8 weeks
Secondary HbA1c changes from baseline and after supplementation 8 weeks
Secondary dermal glycation by skin fluorescence changes from baseline and after supplementation 8 weeks
See also
  Status Clinical Trial Phase
Completed NCT03093792 - Effects of Diet Manipulation on Women in the Curves Program N/A
Active, not recruiting NCT04230928 - Giving a Low Carbohydrate Diet to Overcome Hypertension N/A