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Role of Ayurveda drugs (Vedvidhya Vati and Darvyadi Kwatha) in management of Diabetes.

Randomized Comparative Clinical Study to Evaluate the Efficacy of Vedvidya Vati with and without Darvyadi Kwatha in the Management of Madhumeha w.s.r. to Type 2 Diabetes Mellitus

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/08/020821
Enrollment
40
Registered
2019-08-21
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

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

Interventions

Intervention1: Vedvidya Vati: 20 patients will be administered trial drug Vedvidya Vati 250 mg orally twice a day, 30 minutes before meals for 30 days with lukewarm water. Intervention2: Vedvidya Vati

Sponsors

National Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient willing to sign the consent form. 2. Patients with Fasting Blood Sugar (FBS) in the range of 126mg/dl â?? 250mg/dl or Post Prandial Blood Sugar (PPBS) in the range of 200mg/dl â?? 300 mg/dl.

Exclusion criteria

Exclusion criteria: 1. Patients having Type 1 DM. 2. Patients of Type 2 DM who are on insulin therapy. 3. Patients having any serious illness like coronary artery disease, malignancy, kidney failure etc. 4. DM with complications. 5. Pregnant women and lactating mother.

Design outcomes

Primary

MeasureTime frame
Changes in Blood Glucose level.Timepoint: 0th, 15th and 30th day

Secondary

MeasureTime frame
1. Relief in qualitative parameters. (Prabhuta mutrata, Trishnadhikya, Svedadhikya, Kshudhadhikya, Atinidra, Kara-pada-tala daha, Kara-pada-tala suptata. 2. Changes in lipid profile. Timepoint: 0th day and 30th day

Countries

India

Contacts

Public ContactDr Shankar Gautam

National Institute of Ayurveda

dr.shankar.ayu@gmail.com8302148804

Outcome results

None listed

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