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Oral Ivermectin for Chikungunya Viral Infection

A Randomized Controlled Trial of Oral Ivermectin for Patients With Chikungunya Viral Infection During Urban Outbreak in Southern Thailand

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06259383
Enrollment
120
Registered
2024-02-14
Start date
2018-01-01
Completion date
2024-01-26
Last updated
2024-02-14

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

Conditions

Clinical Syndrome

Brief summary

Chikungunya viral infection (CVI) is a mosquito-borne infection, caused by chikungunya virus (CHIKV), an alphavirus, belonging to the family Togaviridae. This infection causes febrile illness associated with high fever, rash, acute deliberating and persistent arthralgia. There is no licensed vaccine or specific treatment for this infection. Ivermectin (IVM), commonly-used antiparasitic, has been demonstrated to inhibit replication of CHIKV.

Interventions

DRUGIvermectin

3-day 1 daily dose of 400 μg/kg oral ivermectin

Sponsors

Prince of Songkla University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* patients with virologic confirmation of chikungunya infection who had symptoms less than 72 hours prior to visit

Exclusion criteria

* patients with virologic confirmation of chikungunya infection who had symptoms more than 72 hours prior to visit

Design outcomes

Primary

MeasureTime frameDescription
Day of fever clearance1 week120 participants would be under Body Temperature Assessment - the staff would assess once daily until the fever clearance was below 38C and the measure proportion of patients with fever clearance in each day of assessment until fever clearance at least in 7 days

Secondary

MeasureTime frameDescription
Day of virologic clearance1 week120 participants would be obtained blood examination for virological testing every day until virological clearance at least in 7 days

Countries

Thailand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026