To evaluate effect of munditika churna and Haritaki churna in the management of Vatarakta (gout)

Randomised controlled clinical trial of efficacy of Munditika churna and Haritaki churna in the management of Vatarakta (gout) - NIL

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/09/057542

Enrollment

160

Registered

2023-09-13

Start date

Unknown

Completion date

Unknown

Last updated

2024-04-29

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

Conditions

Health Condition 1: M1A9- Chronic gout, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Participants having classical sign & symptoms of Vatarakta like - 1. Shotha (Swelling) 2. Kathinya (Stiffness & Hardness) 3. Vedanadhikya (Severe pain) 4. Daha (Burning sensation) 5. Toda (Pricking pain) 6. Shyavata & tamrata (Blackish or Coppery) 7. Sphurana (Twitching sensation) 8. Participants having age group between 18 years to 60 years 9. Participants having Serum Uric acid level > 7 mg/dl in Males & >6 mg/dl in Females 10. Participants will be selected irrespective Gender, Religion, Socio-Economic status

Exclusion criteria

Exclusion criteria: 1. Participants having complications like Paka, Khanja, Pangulya and Sandhi vakrata will be excluded. 2. Alcohol and drug abusers, Pregnant and lactating women 3. Symptomatic participants with clinical evidence of Kidney failure 4. k/c/o Malignancy, poorly controlled DM, HTN 5. Participants having other acute or complicated systemic disease which require long term drug treatment

Design outcomes

Primary

Measure	Time frame
Improvement in vatarakta sign & symptomsTimepoint: 15th, 30th, 45th day	—

Secondary

Measure	Time frame
decrease in Hyperuricemia (Sr. Uric acid) levelTimepoint: 45th day	—

Countries

India

Contacts

Public ContactPathan Md Junaid Naim Khan

Pravara medical trusts ayurved college, Shevgaon

sbhagwat.2007@rediffmail.com9922709070

Outcome results