Skip to content

Individualized Homoeopathy vs Rhustox in managment of Chikungunya

Management of Chikungunya with Individualized Homoeopathy vs Rhustox- A single blind Randomized control trial - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/110363
Enrollment
132
Registered
2026-05-11
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: A920- Chikungunya virus disease

Interventions

Intervention1: Individualized Homoeopathic medicine: Individualized homoeopathic remedies in centesimal potencies and appropiate doses will be prescribed for oral administration based on symptom simil
Frequency: as per individualized prescription by the investigator.
Route of administration: Oral.
Duration of intervention: 1 month. Control Intervention1: Rhustox Homoeopathic medicine: Rhustox Homoeopathic medicinewill be employed in 2nd group identified through repertorization. The trial medici
Duration of intervention: 1 month.

Sponsors

Central Council for Research in Homoeopathy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients presenting with acute onset of fever more than 38.5 C and severe arthralgia/arthritis not explained by other medical conditions. 2.Patients having age between 15 to 50 years 3.Patients seropositive for IgM or IgG antibodies. 4.Patients positive for RT-PCR (Reverse Transcriptase Polymerase Chain Reaction) during the first week of illness. 5.Patient of both sexes. 6.Patients providing Written Informed Consent.

Exclusion criteria

Exclusion criteria: 1.Patients diagnosed with Rheumatoid arthritis, osteoarthritis and gout. 2.Patients with complaint of joint pains since 1 to 4 months after H/O Chikungunya infection. 3.Patients below the age of 15 and above 50 years. 4.Immunocompromised patients. 5.Patients on DMARDs. 6.Pregnant women and lactating mother.

Design outcomes

Primary

MeasureTime frame
1.Changes in symptoms of chikungunya using Multi-Dimensional Health Assessment Questionnaire (MDHAQ)Timepoint: Baseline, weekly, till 4 weeks (end of treatment)

Secondary

MeasureTime frame
1. Changes in Visual Analogue Scale (VAS) score of pain on weekly basis till 4 weeks. (end of treatment)Timepoint: From baseline, weekly, till 4 weeks

Countries

India

Contacts

Public ContactHarleen Kaur

Central Council for Research in Homoeopathy

dr.ritikanarula@gmail.com9811281206

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026