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Randomized non-inferiority clinical trial to evaluate the efficacy of a single fixed dose of 18 mg ivermectin for the treatment of uncomplicated strongyloidiasis.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-515968-32-00
Acronym
STRONG-FIX
Enrollment
276
Registered
2024-07-22
Start date
2025-04-08
Completion date
Unknown
Last updated
2025-12-05

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

Conditions

and skin lesions. In situations of low defenses (patients under treatment with corticosteroids, organ transplant recipients or other situations) they can present serious complications with high mortality., respiratory symptoms, Strongyloidiasis is caused by a parasite that is globally distributed in tropical and sub-tropical areas. Most patients with strongyloidiasis are asymptomatic or have mild symptoms with gastrointestinal disturbances

Brief summary

Proportion of patients with microbiological cure at 6 months of treatment.

Interventions

DRUGIVERMECTIN

Sponsors

Fundacio Hospital Universitari Vall D’Hebron Institut De Recerca
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Proportion of patients with microbiological cure at 6 months of treatment.

Countries

Spain

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026