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NCT04126551Completed

Mitochondrial Methylation in Type 2 Diabetes

Unraveling the Role of Mitochondrial DNA Methylation in Type 2 Diabetes

Source: ClinicalTrials.gov · Last updated 7 May 2024

Brief summary (registry, in English)

The overarching goal of this proposal is to determine whether DNA methylation of the mitochondrial DNA impairs mitochondrial function in insulin resistant states such as overweight/obesity and type 2 diabetes.

Status (registry)
Completed
Study type
Observational
Enrollment
27 (actual)
First submitted
11 Oct 2019
Start date
23 Jul 2019
Primary completion date
31 Dec 2023
Lead sponsor
University of Arizona
NCT number
NCT04126551

What you commit to

  • Study type: Observational
  • Participants enrolled: 27
  • From 23 Jul 2019 to the primary completion date, 31 Dec 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Subjects receiving Gemfibrozil must not also be receiving a statin.

Other illness

  • Subjects with a history of clinically significant heart disease (New York Heart Classification greater than grade II; more than non-specific ST-T wave changes on the EKG), peripheral vascular disease (history of claudication), or pulmonary disease (dyspnea on exertion of one flight or less; abnormal breath sounds on auscultation) will not be studied.
  • Recent systemic or pulmonary embolus, untreated high-risk proliferative retinopathy, recent retinal hemorrhage, uncontrolled hypertension, systolic BP\>160, diastolic BP\>95, autonomic neuropathy, resting heart rate \>100, electrolyte abnormalities.

Lab values

  • Subjects must not be receiving any of the following medications: thiazide or furosemide diuretics, beta-blockers, or other chronic medications with known adverse effects on glucose tolerance levels unless the patient has been on a stable dose of such agents for the past three months before entry into the study. Subjects must not be taking estrogens or other hormonal replacement therapy unless the subject has been on these agents on a stable dose for the prior three months. Subjects taking systemic glucocorticoids are excluded. Patients with type 2 diabetes will be excluded if they are taking thiazolidinediones.

Who the study is looking for

  • Subjects must be 21-55 years old
  • Body Mass Index:
    • Lean, healthy BMI ≤25; Overweight,non-diabetic BMI 25-29.9; Obese, non-diabetic BMI 30-50; Type 2 Diabetes (per the American Diabetes Association criteria)
  • Subjects must be able to communicate meaningfully with the investigator and must be legally competent to provide written informed consent.
  • Female subjects must be non-lactating and will be eligible only if they have a negative pregnancy test throughout the study period, and must agree to use acceptable birth control (hormonal contraceptives, barrier methods, have an intrauterine device, or surgical sterilization)
  • Subjects must have the following laboratory values:
    • Hematocrit ≥ 35 vol%
    • Serum creatinine ≤ 1.6 mg/dl
    • AST (SGOT) \< 2 times upper limit of normal
    • ALT (SGPT) \< 2 times upper limit of normal
    • Alkaline phosphatase \< 2 times upper limit of normal
    • Triglycerides \< 150 mg/dl for nondiabetics
    • Triglycerides \<300 for diabetics
    • INR ≤ 1.3
    • HbA1c ≤ 10

Age in the registry: 21 years to 55 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Clinical and Translational Research Center (CaTS)
Coordinator of this site? Confirm its status
TucsonUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.