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A Diagnostic clinical study to evaluate Vyadhi Vipareeta Upashaya in Apathyanimittaja Madhumeha purvarupa, Pre Diabetes

A diagnostic randomized placebo controlled clinical trial to evaluate Vyadhi Vipareeta Upashaya in Apathyanimittaja Madhumeha Purvarupa, Pre-Diabetes - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/062671
Enrollment
60
Registered
2024-02-15
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: R730- Abnormal glucose

Interventions

None listed

Sponsors

Central Council for Reaserach in Ayurvedic Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of age group between 30-50yrs fulfilling diagnostic criteria irrespective of gender, religion, socio-economic status Patients having signs & symptoms of Prameha Purvarupa(Pre-diabetes) Patients having positive results FPG-100 -125 mg/dl, PPG-140-199 mg/dl, HbA1C-5.7-6.4% WHO1 Patients having BMI >25 Patients not on anti-diabetic medications

Exclusion criteria

Exclusion criteria: Patients aged below 30yrs & above 50yrs Type 1DM, Chronic cases of T2DM with known complications (Diabetic Neuropathy, Nephropathy, Retinopathy, Ketoacidosis, wounds) Currently on anti-diabetic medications-insulin Systemic & auto immune diseases- Hypertension, Cardiovascular diseases, Gastro-intestinal disease, Hepatitis, HIV, PCOS Hormonal therapy Pregnant women, lactating mothers

Design outcomes

Primary

MeasureTime frame
To assess changes in the grading of clinical features of Apathyanimittaja Madhumeha Purvarupa, prediabetes, 15DHRQoL index, etiological factors- before and after administration of Vyadhi Vipareeta UpashayaTimepoint: The outcome assessment will be done on day 0, day7, day15, day 30 of the study

Secondary

MeasureTime frame
To assess overall well being of the subjects, guidance about lifestyle, diet changesTimepoint: from day 0 the study to day 30 of the follow up period

Countries

India

Contacts

Public ContactRaj Agrawal

Rajiv Gandhi University of Health Sciences, Bengalauru, Karnataka

drrashmibv@sdmayurbangalore.in9739566112

Outcome results

None listed

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