A Clinical Trial To Study The Effect Of Nithya Virechana In The Patients Of Rheumatoid Arthritis

A Clinical Study To Evaluate The Effect Of Nithya Virechana On Range Of Movements In Amavata w s r To Rheumatoid Arthritis - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/08/072381

Enrollment

Registered

2024-08-12

Start date

Unknown

Completion date

Unknown

Last updated

2024-08-19

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

Conditions

Health Condition 1: M059- Rheumatoid arthritis with rheumatoid factor, unspecified Health Condition 2: M059- Rheumatoid arthritis with rheumatoid factor, unspecified Health Condition 3: M069- Rheumatoid arthritis, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Patients fulfilling diagnostic criteria of Rheumatoid arthritis/Amavata Patients aged between 35-60 years Patients who are fit for Nithya virechana karma

Exclusion criteria

Exclusion criteria: Patients with systemic illness like Diabetes Mellitus Hypertension which will hamper the treatment Pregnancy and Lactating women All autoimmune disorder other than Rheumatoid arthritis

Design outcomes

Primary

Measure	Time frame
Reduction in stiffness , Pain Changes in visual Analogue Scale,Chronic Pain Grade Scale Timepoint: 7 Days	—

Secondary

Measure	Time frame
Relief in all other symptoms of Rheumatoid Arthritis like pain , swelling , joint stiffnessTimepoint: 7 days	—

Countries

India

Contacts

Public ContactDr Deeksha Nayaka H V

Rajiv Gandhi University Of Health Sciences,Bengaluru

kanthipk03@gmail.com9844469138

Outcome results