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Nutritional Therapy for Diabetic Cardiomyopathy

Nutritional Therapy for Diabetic Cardiomyopathy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01373814
Enrollment
22
Registered
2011-06-15
Start date
2010-09-03
Completion date
2011-06-17
Last updated
2024-01-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

T2DM (Type 2 Diabetes Mellitus)

Brief summary

The goal of this study is to determine if nutritional therapy can effectively treat/prevent T2DM and its consequent cardiomyopathy.

Interventions

None listed

Sponsors

Washington University School of Medicine
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
35 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Subjects must be \>30 and \<65 years of age, in order to limit the confounding affect of age on our endpoints. * Subjects must have an ejection fraction \>45% (based on their echocardiogram) * Patients with T2DM and nonalcoholic fatty liver disease or steatohepatitis may be included since they have extensive evidence of steatosis.

Exclusion criteria

* Subjects who have had a myocardial infarction or resting ischemia (by history or as evidenced by hypo/akinesis on the pre-intervention echocardiogram) will be excluded because hypo/akinesis would affect our endpoints of LV mass and diastolic function. * Subjects who are unstable, not able to lie flat for the imaging studies, unable to give informed consent, pregnant, lactating, with atrial fibrillation (which would compromise measurement of E'), or current smokers will be excluded. * Subjects with other major systemic diseases per their clinical charts, history, physical exam, or significant renal insufficiency will also be excluded, as these other system diseases may affect our study endpoints and subject follow-up. * We will exclude patients with significant LV systolic dysfunction (ejection fraction \<45%) * We will not exclude patients with sleep apnea because it does not detrimentally affect LV diastolic function. * Subjects will be excluded a priori if they have any history or evidence of liver disease other than NAFLD, consumed \>20 g alcohol per day.

Design outcomes

Primary

MeasureTime frameDescription
cardiac function2 weekscardiac function as measured by echocardiography incl. tissue Doppler

Secondary

MeasureTime frameDescription
liver steatosis2 weeksliver fat content as measured using MR spectroscopy
myocardial steatosis2 weeksfat in heart muscle as measured using MR spectroscopy
lipidomics2 weeksmass spectroscopy measures of plasma lipid species

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026