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Dietary formulation for Diabetes

Clinical efficacy of a unique dietary formulation in type 2 diabetes. - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/066629
Enrollment
100
Registered
2024-05-01
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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.Swati Mohite
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Participants with Type 2 Diabetes mellitus on Oral Hypoglycemic Agents or insulin for at least 4 weeks that is not anticipated to change during the study. Participants with Type 2 diabetes without medication HbA1c = 6.5 Participants willing for inclusion in clinical trial.

Exclusion criteria

Exclusion criteria: Any neurological condition requiring urgent medical intervention. Any other serious systemic disease in last 3 months. Subjects having malignancies, serious infections as well as those requiring long term steroids and hormonal treatment. Pregnant and lactating women. Subjects having H/O renal transplant.

Design outcomes

Primary

MeasureTime frame
Reduction in Fasting & postprandial blood sugar level Reduction in HbA1c Timepoint: Baseline 30th and 60th

Secondary

MeasureTime frame
Weight loss Reduction in abdominal, chest & hip circumference Timepoint: Baseline 30th 60th and 90th day

Countries

India

Contacts

Public ContactProf Dr Swati Mohite

Bharati Vidyapeeth (Deemed to be University)

dr.ssmohite@gmail.com9822004562

Outcome results

None listed

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