Skip to main content
Clinical Trials/CTRI/2023/08/056521
CTRI/2023/08/056521Not yet recruitingPhase 2/3

A comparative pharmaceutico analytical and clinical study of Rasnasaptak Kashaya And Rasnapanchak Kashaya Ghanvati in Amavata w.s.r.to Rheumatoid Arthritis

Government Ayurvedic College Patiala1 site in 1 country60 target enrollmentStarted: August 26, 2023Last updated:

Trial Snapshot

Phase
Phase 2/3
Status
Not yet recruiting
Sponsor
Enrollment
60
Locations
1
Primary Endpoint
Subjective Parameter- Grading will be done with sign & symptoms of Amavata

Study Overview

Brief Summary

In this trial we are selecting patients of Amavata in two groups, in which we will do intervention study of study with Rasnasaptak kashaya ghanvati and Rasnapanchak kashaya ghanvati with the dose of two tablets of 500 mg BD assesment will be done on the subjective and objective parameters for the Amavata.

Route of Drug Adminitration - Oral

Follow up- Day 10, day 20, day 30

Study Design

Study Type
Interventional
Allocation
Not Applicable
Masking
Open Label

Eligibility Criteria

Ages
20.00 Year(s) to 70.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Patient willing for trial
  • Either Sex will be selected
  • Newly Diagnosed case and patient not on any medication since one month will be selected
  • Patient having classical symptoms of Rheumatoid Arthritis will be Selected.

Exclusion Criteria

  • Age more than 70 yrs and less than 20 yrs.
  • Patient not willing for trial.
  • Pregnancy and lactating mothers
  • Patients suffering from any known case of severe systemic disorder like Crohn Disease, SLE, Graves disease, AIDS etc, which may interfere with the course of treatment will be excluded.

Outcomes

Primary Outcomes

Subjective Parameter- Grading will be done with sign & symptoms of Amavata

Time Frame: After one month intervention of Rasnasaptak kashaya Ghanvati and Rasnapanchak kashaya Ghanvati orally.

RA factor,ESR,CRP,SGOT,SGPT,Uric Acid,HB,TLC to rule out other pathologies

Time Frame: After one month intervention of Rasnasaptak kashaya Ghanvati and Rasnapanchak kashaya Ghanvati orally.

Secondary Outcomes

  • Subjective parameter-grading will be done with sign & symptoms of Amavata RA factor, ESR,CRP,SGOT,SGPT,Uric acid,HB(After one mmonth intervention of Rasnasaptak Kashaya Ghanvati & Rasnapanchak Kashaya Ghanvati)

Investigators

Sponsor
Government Ayurvedic College Patiala
Sponsor Class
Government medical college

Study Sites (1)

Loading locations...

Similar Trials