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A Clinical Trial to Study the Efficacy of Vedanasthapana Gana Kashaya (An Ayurvedic Decoction) in Subjects With Different Kinds of Pain.

Analytical Study On Vedana (Pain) Vis-A-Vis Assesment of The Role of Vedanasthapana Gana Dravya in Pain Management. - NIL

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/058332
Enrollment
100
Registered
2023-10-05
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Health Condition 1: R079- Chest pain, unspecified Health Condition 2: G439- Migraine, unspecified Health Condition 3: M472- Other spondylosis with radiculopathy Health Condition 4: R52- Pain, unspecified Health Condition 5: R109- Unspecified abdominal pain

Interventions

None listed

Sponsors

Dr.Sharanabasappa policepatil
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Subjects fulfilling diagnostic criteria. 2. Subjects between the age group of 20-60years will be selected 3. Known case of HTN and DM with strict control of Blood pressure and blood glucose level will be selected.

Exclusion criteria

Exclusion criteria: 1. Subjects suffering from chronic systemic disorders and subjects on other medications which interrupt the study. 2. Pregnant women. 3. Diabetic patient with uncontrolled blood glucose level. ? Hypertension patient with uncontrolled Blood pressure. ? Subjects with acute abdominal pain. ? Patients with pain requiring surgical intervention and acute management.

Design outcomes

Primary

MeasureTime frame
Assessment of vedanasthapana dashamani kashaya in different type of pain ardhava bhedaka grivasthisandigataavata udarashula parsvashula angamarda before & after interventionTimepoint: Day 8

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDrSharanabasappa policepatil

Government Ayurveda medical college and hospital mysuru

vachate37@gmail.com9448150212

Outcome results

None listed

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