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Clinical Trials/NCT01802541
NCT01802541
Completed
Not Applicable

Effect of Diacylglycerol Oil on Risk Factors of Type 2 Diabetes and Complicating Disease, and Mechanism

Zhejiang University0 sites127 target enrollmentMarch 1, 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Insulin Sensitivity
Sponsor
Zhejiang University
Enrollment
127
Primary Endpoint
insulin resistance
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

Diacylglycerol oil has been shown to lower postprandial and fasting serum triacylglycerol levels and reduce body fat. The investigators hypothesize that replacing dietary fat with diacylglycerol oil reduces excess body fat in type 2 diabetic patients and that diacylglycerol oil has a beneficial effect on cardiovascular risk factors in Chinese type 2 diabetic patients.

Registry
clinicaltrials.gov
Start Date
March 1, 2013
End Date
February 2006
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Zhejiang University
Responsible Party
Principal Investigator
Principal Investigator

Duo li

Professor

Zhejiang University

Eligibility Criteria

Inclusion Criteria

  • Type 2 diabetic patients, blood sugar levels were stabilized between 7.0-10.0 mmol/L
  • Male, aged 40 - 70 years old, Female, aged post-menopausal - 70 years old.
  • Overweight/obese patients (BMI 25 - 40 kg/m2)
  • Currently under diet therapy for diabetes mellitus
  • Understands the procedures and willing to participate in the study

Exclusion Criteria

  • Patients who unwilling to give informed consent
  • Type 1 diabetic patients
  • Familial hyperlipemia patients or blood triacylglycerol concentration \> 400 mg/dl
  • Patients with a history of cardiovascular disease and/or arteriosclerotic disease
  • Patients with a history of cerebrovascular disease
  • Patients with serious hepatic disease and/or renal disease
  • Patients with malignancy
  • Participation in another clinical study within 30 days prior to screening period.
  • Has a condition the doctor in charge believes would interfere with evaluation of the subject, or may put subject at undue risk

Outcomes

Primary Outcomes

insulin resistance

Time Frame: 120 days

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