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Clinical Trials/CTRI/2024/06/068864
CTRI/2024/06/068864CompletedPhase 2/3

A Pharmaco-Therapeutic Study of Varun and Indrayava in Vatarakta w.s.r to Gout

Government Ayurvedic College and Hospital Patna Aryabhatta Knowledge University Patna Bihar1 site in 1 country60 target enrollmentStarted: June 24, 2024Last updated:
Conditions
Drugs

Trial Snapshot

Phase
Phase 2/3
Status
Completed
Sponsor
Enrollment
60
Locations
1
Primary Endpoint
Improvement in the patient will be assessed mainly on the basis of relief in cardinal symptoms of disease. To access the effect of drug therapy subjectively, all sign & symptoms will be relief in

Study Overview

Brief Summary

Vatarakta is a chronic  is a chronic and complex metabolic disorder of musculoskeletal system and characterised by severe pain, tenderness, inflammation and burning sensation in the affected joints. Vatarakta is a Vatapradhana Vyadhi where Rakta is main Dushya. The drug used in this trial is Varun churna and Indrayava churna  mentioned in Ayurveda text with hope that they will prove more efficacious, less toxic and easy to use. This drug is easily available and  effective in Vatarakta. Patient will be taken from OPD and IPD of Government Ayurvedic College and Hospital Patna. Duration of trial is 30 days.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
20.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • •Patient willing for Trial.
  • •Patient having symptoms of Vatarakta vyadhi as per ayurvedic classic and Gout w.s.r to modern view have include under the study.
  • •Patient having age between 20-60 year who can present their sign and symptoms of Vatarakta.

Exclusion Criteria

  • •Patients who have HIV HCV CKD etc Patients suffering from serious systemic disorder like Diabetes Renal Calculus Hepatic Disorder are excluded Cardiac patients Cancer patient On Chemotherapy patient On Dialysis patient are excluded Patient who have suffering from serious lungs disorders Asthmaticus Bronchogenic Carcinoma or other types of malignancy Pregnant and Lactating Women Anemia- less than hemoglobin 9mgdl.

Outcomes

Primary Outcomes

Improvement in the patient will be assessed mainly on the basis of relief in cardinal symptoms of disease. To access the effect of drug therapy subjectively, all sign & symptoms will be relief in

Time Frame: 60 Days (8 weeks)

1. pain in affected joint.

Time Frame: 60 Days (8 weeks)

2. swelling in the affected joint.

Time Frame: 60 Days (8 weeks)

3. law of tactile sensation. upon their severity.

Time Frame: 60 Days (8 weeks)

Secondary Outcomes

  • chaneges in serum uric acid and blood urea(60 days)

Investigators

Sponsor
Government Ayurvedic College and Hospital Patna Aryabhatta Knowledge University Patna Bihar
Sponsor Class
Research institution and hospital
Responsible Party
Principal Investigator
Principal Investigator

Dr Raj Kishor Verma

Government Ayurvedic College and Hospital Patna

Study Sites (1)

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