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Efficacy of Shallakyadi capsule in the prevention of post chikungunya chronic inflammatory rheumatism

Efficacy of Shallakyadi capsule in the prevention of post chikungunya chronic inflammatory rheumatism-a prospective cohort study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/02/023123
Enrollment
81
Registered
2020-02-05
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Health Condition 1: M148- Arthropathies in other specified diseases classified elsewhere

Interventions

Intervention1: shallakyadi capsule: 2 capsules twice daily before meal with luke warm water orally for the duration of 8 weeks Control Intervention1: Shallakyadi Capsule: 2 capsule twice a day before

Sponsors

Institute for Post Graduate Teaching and Research in Ayurveda Gujarat Ayurved University Jamnagar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age between 18 years to 60 years of either sex. Confirm case of Chikungunya fever Patient willing to participate in the trial.

Exclusion criteria

Exclusion criteria: Age below 18 years & above 60 years. ? Pregnant and lactating women ? History of RA, Gout, Psoriatic arthritis, rheumatic fever, autoimmune disease, thyroid dysfunction, sarcoidosis, SLE before Chikungunya fever. ? Patients suffering from: Malignant and accelerated hypertension, coronary artery disease, uncontrolled diabetes. ? Patient undergoing regular treatment for any other severe illness and also patients suffering from pulmonary tuberculosis or bone tuberculosis, carcinoma and HIV positive patients.

Design outcomes

Primary

MeasureTime frame
It is expected that the trial drug will reduce the inflammation and pain through correcting underlined pathogenesis and so that it will become possible to prevent Post-Chikungunya Chronic Inflammatory Rheumatism (pCHIK-CIR).Timepoint: at the end of 8 weeks

Secondary

MeasureTime frame
The drug will improve the quality of life in patient of Chikungunya.Timepoint: 8 weeks

Countries

India

Contacts

Public ContactBineesh E P

Institute for Post Graduate Teaching and Research in Ayurveda Gujarat Ayurved University Jamnagar

kaurmandip22@yahoo.com9427572306

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026