Effect of Indravaruni Choorna in Prameha (high blood sugar levels in body)

A Randomised Controlled Clinical Trial To Study The Effect Of Indravaruni Choorna in Prameha With Special Reference To Diabetes Mellitus Type 2 - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/05/086468

Enrollment

Registered

2025-05-07

Start date

Unknown

Completion date

Unknown

Last updated

2025-05-26

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

Eligibility

Inclusion criteria

Inclusion criteria: a. Patient showing signs and symptoms of Prameha such as Prabhuta Mutrata (polyuria),Avila Mutrata(unclear urine) ,Ati-sweda(sweating), Daurbalya(weakness),Pipasa(polydipsia),Kshudavriddhi (Polyphagia) ,Naktamutrata (Nocturnal urination) b. patient already diagnosed with DM type 2 c. Age 40-60 years. d. Patient having their Fasting blood glucose level range of 120 200 mg/dl. e. Post prandial blood glucose level range of 170 - 250 mg/dl

Exclusion criteria

Exclusion criteria: 1. IDDM, Acromegaly, Cushing s syndrome and Pancreatic disorder. 2. Pregnant and lactating women. 3. Patient with gestational diabetes. 4. Patient suffering from Hepatic dysfunction, Renal dysfunction or Liver cirrhosis. 5. Patient in whom DM is caused as drug induced complication. 6. Those who are under Insulin therapy. 7. Patient with DKA, Lactic acidosis, Sepsis.

Design outcomes

Primary

Measure	Time frame
Reduction in signs and symptoms of Prameha after ingestion of Indravaruni choornaTimepoint: 30 dyas	—

Secondary

Measure	Time frame
Where the trial group stands in comparison with control groupTimepoint: 18 months	—

Countries

India

Contacts

Public ContactDr Sandesh Bhagunath Shinde

SMBT Ayurved college and Hospital

dr.ankush30@gmail.com7359117691

Outcome results