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Active Not Recruiting NCT07876622

Evaluation of the Rapid Diagnostic Test SsRT+ for Strongyloides Stercoralis

Conditions: Strongyloides Stercoralis Infection, Device Performance, Diagnostic

Sex: All
Healthy volunteers: No
Phase: NA
Enrollment: 780
Sponsor: IRCCS Sacro Cuore Don Calabria di Negrar

Location: IRCCS Sacro Cuore Don Calabria Hospital Negrar Verona

Summary

The goal of this performance study is to determine if the diagnostic accuracy of the SsRT+ for the diagnosis of S. stercoralis infection meets the minimum requirements defined in the WHO target product profile. The study does not involve patients, but rather the analysis of samples stored in the local biobank.

Eligibility Criteria

Inclusion Criteria: * Serum from individuals who were prescribed screening tests for S. stercoralis * Written consent to the donation of the leftover sample to the local biobank Exclusion Criteria: * Unavailable/insufficient quantity of serum * Serum from individuals who received treatment with ivermectin in the previous 6 months

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07876622). StuddyBuddy aggregates publicly available trial information.