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A Comparative clinical trial to study the effect of Vaitaran Basti with Gomutra & Vaitarana Basti with Gomutra Arka in the management of Amavata

A Randomized comparative clinical study to evaluate the efficacy of Vaitaran Basti with Gomutra & with Gomutra Arka in the management of Amavata

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/054675
Enrollment
30
Registered
2023-07-03
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

Health Condition 1: M049- Autoinflammatory syndrome, unspecified

Interventions

None listed

Sponsors

Parul Ayurved Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with classical sign and symptoms of Aamavat 2. Amavata patients between age group of 18 to 70 years 3. Patients of either Gender irrespective of Caste and Religion.

Exclusion criteria

Exclusion criteria: 1. Patients of Age below 18 years and above 70 years of either sex. 2. Patients having other systemic disorders â?? (known case of) Hypertension, Carcinoma,Tuberculosis, Infectious diseases and other Life threatening disorders. 3. Patients with extremely reduced joint space. 4. Patients with Bone Deformity 5. Patients contraindicated for Vaitaran Basti Karma. 6. Patients contraindicated for Shodhan such as Pregnant & Lactating women

Design outcomes

Primary

MeasureTime frame
Assessement of Significant improvement of Sign & Symptoms of AmavataTimepoint: 8 days of BastiKarma treatment and follow up Aftet 16 Days

Secondary

MeasureTime frame
Assessment of significant improvement in the sign & symptoms of aamvat & their will improving the life quality of patients of aamvatTimepoint: Assessment After 8 days of treatment & followed up After 16 days.

Countries

India

Contacts

Public ContactDr Nirmala Sonawane

Parul Institute Of Ayurved

ayurved05@gmail.com8329614671

Outcome results

None listed

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