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A study to evaluate effect of consumption of two white rice varieties on Blood glucose in healthy human volunteers

A study to evaluate effect of consumption of two white rice varieties on Glycaemic Index in healthy human volunteers

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/06/008837
Enrollment
50
Registered
2017-06-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

None listed

Interventions

Intervention1: 2 white Rice varieties: Total 68-69 gm of uncooked weight of the test sample will be consumed orally along with 200 ml of drinking water after 10-12 hours of overnight fasting. Each ric

Sponsors

ITC Life Sciences and Technology Center ITC LTD
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Healthy adults (based on medical history and screening tests) age between 18 and 45 years male and female (1:1 ratio) will be enrolled into the study after written informed consent has been obtained. 2.Subject is willing to give written, signed and dated informed consent to participate in the study before initiating any study related procedure. 3.Fasting blood glucose levels less than 100 mg/dl 4.BMI should be between 18.5 to 25 kg/m2 5.Lipid profile (Triglycerides, Cholesterol, LDL, HDL, VLDL) within normal range as applicable to each parameter.

Exclusion criteria

Exclusion criteria: 1.Subjects with BMI less than 18.5kg/m2 or more than 25kg/m2 will be excluded from the study. 2.Fasting blood glucose levels > 100mg/dl. 3.Subjects with Clinically significant Lipid profile values are excluded 4.Subjects particularly on any special diet 5.Subjects suffering with diabetes, cardiovascular, renal, pulmonary, endocrine, or neurological disorders, ulcers, dermatologic disorders, autoimmune diseases or severe food allergies; an active infectious disease (HBV, HCV,HIV); a current diagnosis or a history of relevant depressive episodes or of panic attacks, psychosis, bipolar or eating disorders 6.Pregnant or lactating women 7.Subject having participated in any other clinical trial within one month prior to screening

Design outcomes

Primary

MeasureTime frame
To determine the effect of two white rice varieties on glycaemic indexTimepoint: Screening and each visit—

Secondary

MeasureTime frame
To determine the iAUC of two white rice varietiesTimepoint: Screening and each visit—

Countries

India

Contacts

Public ContactSudha Raj

ITC Life Sciences and Technology Center, ITC LTD,

Yashwanth.Radhakrishnan@itc.in9964358455

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026