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Clinical Trials/CTRI/2019/11/021946
CTRI/2019/11/021946
Not yet recruiting
未知

Study to Compare and evaluate the Glycemic index of commercially available breakfast food items related to its effect in achieving better glycemic control in diabetic and non-diabetic patients.

Bangalore Diabetes Centre0 sites0 target enrollmentTBD
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Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Bangalore Diabetes Centre
Status
Not yet recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Bangalore Diabetes Centre

Eligibility Criteria

Inclusion Criteria

  • •1\.Type II Diabetes Mellitus and Non diabetic subjects of either sex aged 18 to 60years.
  • •2\.Type II Diabetes Mellitus subjects with duration less than 5 years.
  • •3\.Subjects able to provide written informed consent.
  • •4\.Subjects without any antidiabetic medication or on metformin as monotherapy
  • •5\.Agree to follow the study prodecures and adhere to visits.
  • •6\.If female of childbearing age, willing to use an acceptable form of birth control measure, should be stable for past 3 months prior to baseline and throughout the study.

Exclusion Criteria

  • •1\.Subjects with deteriorating health status at the time of enrolment; rapid weight loss, terminal disease, significant chronic disease (e.g., chronic diarrhea, gastro\-intestinal disease, irritable bowel syndrome).
  • •2\.Type II Diabetes Mellitus subjects with duration more than 5 years.
  • •3\.Recent blood donation (within 3 months from the date of screening).
  • •4\.Immunodeficiency disease (e.g., human immunodeficiency virus \[HIV] infection).
  • •5\.Pregnant or breast feeding women.
  • •6\.Currently participating or having participated in another clinical trial during the last 3 months prior to the beginning of this study.
  • •7\.Conditions in the opinion of the investigator make the patient unsuitable to participate in the study .
  • •8\.Any contraindication to blood sampling.
  • •9\.Subjects with history of nephropathy/Renal dysfunction.

Outcomes

Primary Outcomes

Not specified

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