Skip to content

Effect of a New Finger Millet Drink on Blood Sugar Control in Type 2 Diabetes

Efficacy of Novel Finger Millet Beverage on Glycemic regulation in Type 2 Diabetes Mellitus - A Randomized Controlled Clinical Study - NIL

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/085316
Enrollment
60
Registered
2025-04-22
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: E119- Type 2 diabetes mellitus without complications

Interventions

None listed

Sponsors

Dr. Gunjana Atreya
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Aged 30-70 Years(both male and female) 2) Individuals diagnosed with type 2 diabetes mellitus 3) Patient willing to give written consent 4) 8 hours fasting blood sugar greater than 126mg/dl and less than or equal to 250mg/dl Or, 5) 2-hour postparandial blood sugar greater than 200mg/dl and less than or equal to 350mg/dl Or, 6) HbA1C level greater than or equal to 4.8mmol/l or (6.5%) and less than or equal to 13.4mmol/l or (10%) Note: Point 4,5,6 any one from this if present will be included along with the above 1,2,3 points.

Exclusion criteria

Exclusion criteria: 1) Individuals with type 1 diabetes mellitus 2) Pregnanat or lactating women 3) Those with sever comorbidities affecting dietary intake or metabolism 4) Individuals with allergies or intolerance to finger millet.

Design outcomes

Primary

MeasureTime frame
Parameter to be assessed are as follows: Objective Criteria Fasting and Post blood glucose level HbA1c Anthropometric data(height, weight, BMI, waist circumference, hip circumference, etc) Subjective Criteria Polyuria Polydipsia Fatigue Timepoint: Time of assessment of respective parameter will be done as follows: Fasting and Post blood glucose level will be tested at baseline,4th weeks,8th weeks,and 12th weeks. HbA1C will be estimated at baseline and 12th weeks. Anthropometric data and Subjective criteria at every 15 days once until 90 days

Secondary

MeasureTime frame
NILTimepoint: Not Applicable

Countries

India

Contacts

Public ContactDr Dhaivat Vora

Parul Institute of Ayurved & Research, Parul University, Vadodara, Gujarat

dhaivat.vora17591@paruluniversity.ac.in9879287123

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026