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Clinical Trials/CTRI/2019/04/018362
CTRI/2019/04/018362
Not yet recruiting
未知

An open label crossover study to estimate Glycemic index of Murchit Atta as compare to Regular Atta in a patients with Type 2 Diabetes mellitus

Madhavbaug Multidisciplinary Cardiac Care Clinics and Hospital0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: E119- Type 2 diabetes mellitus without complications

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: E119- Type 2 diabetes mellitus without complications
Sponsor
Madhavbaug Multidisciplinary Cardiac Care Clinics and Hospital
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
Madhavbaug Multidisciplinary Cardiac Care Clinics and Hospital

Eligibility Criteria

Inclusion Criteria

  • •1\. Patients of either sex in the age group between 18 to 50 years (Both Inclusive)
  • •2\. Willing to provide written informed consent
  • •3\. Patients diagnosed to be suffering from Type 2 diabetes mellitus taking oral hypoglycemic drugs and with blood sugar stabilized within normal range(Fasting sugar level \< 110 mg/dl and Postprandial sugar level \< 140 mg/dl )

Exclusion Criteria

  • •1\.Patients of either sex having age below 18 and above 50
  • •2\. Not willing to provide written inform consent
  • •3\. Patients diagnosed as Type 1 diabetes mellitus
  • •4\. Patients with past 30 days history
  • •A) Any major illness that required hospitalization
  • •B) acute exacerbation of any ongoing chronic medical illness e.g. Congestive cardiac failure Hepatitis Hypotensive episodes HIV etc Medications requiring change of doses for treatment of the chronic illness
  • •5\. Patients suffering from severe cardiac renal liver or any other organ impairment.
  • •6\. History of seizures epilepsy or any neurological disorders
  • •7\. Recent history of dehydration from diarrhoea vomiting or any other reason within a period of 24 hours prior to enrolment in the study
  • •8\. Patient with any history of food allergy or any ingredient of investigational Murchit atta

Outcomes

Primary Outcomes

Not specified

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