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A clinical study of nutritional and phytoconstituents supplementation in prediabetic subjects

A Randomized, placebo controlled study to assess the efficacy & safety of nutritional and phytoconstituents supplementation in prediabetic subjects - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/12/047809
Enrollment
300
Registered
2022-12-01
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-01

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

Conditions

Health Condition 1: R739- Hyperglycemia, unspecified

Interventions

Intervention1: Diabetone tablet along with Cinafen plus tablet.: One tablet of each Diabetone and Cinafen plus daily after main meal with lifestyle modifications for 90 days. Control Intervention1: Pl

Sponsors

Meyer Organics Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Male and female subjects of 30 to 60 years of age (both inclusive) 2. BMI >=28.00- 3. Hemoglobin A1c (HbA1c) >=5.7 % and 4. Fasting Plasma Glucose (FPG) between 100-125 mg/Dl both inclusive.

Exclusion criteria

Exclusion criteria: 1. Subjects with type 1 or type 2 diabetes mellitus (T2DM), gestational diabetes (GDM), or secondary diabetes; 2. Treatment with glucose lowering agent (s) within 90 days before screening. 3. Subjects with elevated liver enzymes AST and/or ALT >3 times of the upper normal limit 4. Subjects with abnormal renal function as measured by eGFR 5. Subjects with BMI more than 35Kg/m2 6. Subjects who had a bariatric surgery. 7. Pregnant or lactating women. 8. Smokers/Alcoholics and/or drug abusers. 9. Subjects with known history or ongoing malignancy. 10. Treatment with immunosuppressive medications in past three months. 11. Subjects suffering from major systemic illness necessitating medical care. 12. Any other reason which can affect the participation of the subject in the study as per investigatorâ??s discretion.

Design outcomes

Primary

MeasureTime frame
1. HbA1c, fasting and post meal plasma glucose levels from screening to end of the study. 2. HOMA-IR score (calculated insulin resistance based on formula with fasting plasma glucose and fasting serum insulin levels) at screening and end of the study.Timepoint: Screening to end of the study

Secondary

MeasureTime frame
1. Anthropometric parameters like body weight, BMI and % body fat by impendence test at screening and end of the study. 2. Changes in lipid profile at screening and end of the study. 3. Changes in perceived stress score at screening and end of the study. 4. Changes in HRQOL-15D questionnaire score to assess quality of life at screening and end of the study.Timepoint: Screening to end of the study

Countries

India

Contacts

Public ContactNeepa Gaba

Meyer Organics Pvt. Ltd.

rmamsa@meyer.co.in9167846090

Outcome results

None listed

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