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To See the efficacy of Katankateryadi kwatha and Indra Vati in the management of Madhumeha (Diabetes mellitus)

A clinical study to evaluate efficacy of Katankateryadi kwatha and Indra Vati in the management of Madhumeha w.s.r. to Type II Diabetes mellitus.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/06/019627
Enrollment
45
Registered
2019-06-11
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: Katankateryadi Kwatha: Patients in Group A will be administered Trial Drug Katankateryadi Kwatha in the dose of 50 ml BD before meal for 30 days. Intervention2: Indra Vati: Patients in

Sponsors

National Institute of Ayurveda Jaipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: i.Patient willing to sign the consent form. ii.Patients between the ages of 30-70 years of either sex. iii.Patients giving the clinical history of DM (Type II). iv.Patients having hyperglycemia confirmed by laboratory investigations i.e. Fasting Blood Sugar (FBS) >= 126mg/dl or Post Prandial Blood Sugar (PPBS) >= 200mg/dl or Glycosylated Hemoglobin (HbA1c) >= 6.5%. v.Presence of Cardinal symptoms of Diabetes Mellitus eg. (3P- polyuria, polydypsia, polyphagia).

Exclusion criteria

Exclusion criteria: i.Patients below 30years of age & above 70 years of age. ii.Patients having Type I DM. iii.Patients of Type II DM who are on insulin therapy. iv.Patients having any serious illness like Coronary Artery Disease, malignancy, etc. v.Drug induced DM. vi.F.B.S. > 200 mg/dl and P.P.B.S. > 300 mg/dl. vii.Patients having chronicity of more than 5 years. viii.DM with complications. ix.Pregnant and lactating mother.

Design outcomes

Primary

MeasureTime frame
Assessment of changes in specific signs and symptoms of Madhumeha and Type II Diabetes MellitusTimepoint: 30 days for Each Patients

Secondary

MeasureTime frame
Any adverse effect in the values of haematological test and in clinical signs and symptoms.Timepoint: 30 days for Each Patients

Countries

India

Contacts

Public ContactDr Harish Bhakuni

National Institute of Ayurveda

joshirk1964@gmail.com9414322297

Outcome results

None listed

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