Skip to content

A clinical Study on the Blood Sugar Lowering Effects of Pashanbheda (Bergenia ligulata) in Type 2 Diabetes

Phytochemical and Exploratory Clinical study to evaluate the hypoglycemic effect of Pashanbheda (Bergenia ligulata Wall.) with special reference to Prameha (Diabetes mellitus type 2) - NIL

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/108840
Enrollment
60
Registered
2026-04-20
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Sponsors

Post Graduate Institute of Ayurveda DSRRAU Jodhpur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients between the age group of 30-70 years, of either sex, with clinical features of Prameha (Diabetes mellitus type2). 2. Patients having a fasting blood sugar level (FBS) greater than 126 mg/dL and less than 200 mg/dL and patients having a 2 hour post prandial blood sugar level (PPBS) greater than 200mg/dL and less than 350 mg/dL. 3. Patients with HbA1c range 6.4 or more. 4. Written consent showing willingness to participate in the study. 5. Freshly diagnosed patient (with no other hypoglycemic treatment).

Exclusion criteria

Exclusion criteria: 1. Patients below the age of 30 years and above 70 years will be excluded. 2. Pregnant and lactating mothers. 3. Known case of Type 1 Diabetes Mellitus or I. D. D. M. Patients are excluded. 4. Type 2 DM patients having insulin therapy due to secondary failure. 5. Patients suffering from the complications of DM like Ketoacidosis, Neuropathy, Nephropathy, Retinopathy and Diabetic wounds. 6. Patients suffering from any severe systemic disease, chronic infections or any active malignancy.

Design outcomes

Primary

MeasureTime frame
Changes in the Objective parameters.Timepoint: 90 days

Secondary

MeasureTime frame
Changes in the clinical sign and symptoms of Prameha (Type 2 DM)Timepoint: 90 days

Countries

India

Contacts

Public ContactDr Jahanvee gautam

PGIA, DSRRAU, Jodhpur

drmanojarora2503@gmail.com9166639579

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026