Effect of 1 25-dihydroxyvitamin D3 Treatment on Insulin Secretion and Muscle Strength in Pre-diabetic Persons

  • STATUS
    Not Recruiting
  • participants needed
    75
  • sponsor
    Mayo Clinic
Updated on 19 February 2024
body mass index
insulin
fasting
serum glucose
prediabetic state

Summary

The aim of this study is to assess the effects of 1,25(OH)2D3 on insulin secretion by the pancreas and glucose utilization by skeletal muscle as well as to determine the effects of 1,25(OH)2D3 on muscle strength in pre-diabetic persons

Details
Condition Prediabetes
Age 20-45 years
Treatment Oral Placebo, Calcitriol capsules
Clinical Study IdentifierNCT04286529
SponsorMayo Clinic
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

b'Body mass index (BMI) of >24kg/m2'
b'Fasting serum glucose <126 mg/dL'

Exclusion Criteria

b'BMI</=24 kg/m2'
b'Fasting serum glucose >/=126 mg/dL'
b'Patient is taking Calcium or Vitamin D supplements and is unwilling to stop for 8'
b'weeks'
b'Serum Calcium >10.2 mg/dL'
b'Serum inorganic phosphorous >4.5mg/dL'
b'Pregnancy or breastfeeding'
b'Diagnosis of Diabetes Mellitus'
b'Diagnosis of Rheumatoid Arthritis'
b'Diagnosis of Chronic Obstructive Pulmonary Disease (COPD)'
b'Renal in sufficiency/failure ( serum creatinine >1.5 mg/dL men, > 1.3 mg/dL women)'
b'Chronic active liver disease (bilirubin >1.2 mg/dL, AST>144IU/L, or ALT >165 IU/L)'
b'History of chronic hepatitis'
b'Active coronary artery disease ( unstable angina, myocardial infarction, stroke and'
b'revascularization of coronary, peripheral or carotid artery within the last 3 months)'
b'Oral warfarin group medications or history of blood clotting disorders'
b'Platelet count <100,000 per uL within the last 7 days'
b'Alcohol consumption greater than 2 glasses/day or other substance abuse'
b'Untreated or uncontrolled thyroid disorders (outside a TSH range of 0.5 to 10mIU/L)'
b'Debilitating chronic disease (at the discretion of the investigators)'
b'The presence of infections, highly communicable diseases ( AIDS, active tuberculosis,'
b'venereal disease, hepatitis)'
b'Any malignancy'
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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