MedPath

to compare the efficiency of some herbal drugs in the treatment of amavata

Phase 2
Completed
Conditions
amavata ( rheumatoid arthritis)
Registration Number
CTRI/2017/12/010844
Lead Sponsor
National Institute of Ayurved
Brief Summary

The clinical presentation of Amavata closely mimics with the special variety of Rheumatologic disorders called rheumatoid arthritis (R.A.). Prevalence of RA is approx. 0.8 % of the population. Due to wide spectrum of disease, much prevalence in the society and lack of effective medicine, the disease had been chosen for the study. Aim- To compare the efficacy of “Shiva Guggulu†and “Alambushadi Ghan Vati†in the management of Amavata (R.A.). Settings and Design: Single Centered, Open Labeled, Randomized Clinical Study. Methods and Material: 50 clinically diagnosed

patients of Amavata and who fulfilled the criteria of inclusion and willing to participate in trial were registered for present clinical trial and divided into two groups by simple randomization method (Lottery method). Group A- 25 patients of Amavata were administered ‘Shiva Guggulu’ 2 Tab (each Tab 500 mg.) thrice in a day with lukewarm water, after meal for 30 days Group B- 25 patients of Amavata were administered ‘Alambushadi Ghan Vati’ 2 Tab (each Tab 500 mg) thrice in a day, with lukewarm water, after meal for 30 days. Statistical analysis used: In Stat Graph Pad 3 Software was used for statistical analysis. For Nonparametric data Wilcoxon matched-pairs signed ranks test while for Parametric data Paired‘t’ Test and for Inter group comparison, Mann-Whitney Test & Unpaired ‘t’ Test were used. Conclusion: On comparing the effect of two therapies it can be concluded that Group B (Alambushadi Ghana Vati) provided better relief statistically than Group A (Shiva Guggulu) in most of the sign and symptom of the disease. It also considerably prevents the relapse.

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
50
Inclusion Criteria
  • The patients between the age group of 16 to 60 years in either sex presenting with clinical features of Amavata (R.A.).
  • Pre-diagnosed patient of Amavata.
  • (Chronicity < 4 years) 3.
  • Patient willing to sign the consent forms.
Exclusion Criteria
  • Patients having severe crippling bone deformities.
  • Patients suffering from paralysis.
  • Patients having any type of arthopathy such as neoplasm of spine, Gout, Ankylosing spondylosis, traumatic arthritis and pyogenic Osteomylitis etc.
  • Patients having associated Cardiac disease, Tuberculosis, Diabetes Mellitus, Malignant Hypertension, Renal Function Impairment; Hypothyroidism, RHD etc.
  • Patients with extremely reduced joint space.
  • Pregnant women and lactating mother.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Patients of either sex 16-60 yr old diagnosed with amavata (rheumatoid arthritis) will be selected for relief in sign and symptoms30 days
Secondary Outcome Measures
NameTimeMethod
Assess comparative efficacy of shiva gutika and alambushadi ghan vati in amavata (rheumatoid arthritis)30 days

Trial Locations

Locations (1)

National Institute of Ayurveda

🇮🇳

Jaipur, RAJASTHAN, India

National Institute of Ayurveda
🇮🇳Jaipur, RAJASTHAN, India
Prof Ram Kishor Joshi
Principal investigator
9414322297
joshirk1964@gmail.com

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