Skip to content

Assessment of infection activity in travelers and migrants diagnosed with chronic schistosomiasis: a multicentric prospective cohort study

Assessment of infection activity in travelers and migrants diagnosed with chronic schistosomiasis: a multicentric prospective cohort study - SchistACT (Schistosomiasis ACTive & ACTion)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON57449
Enrollment
15
Registered
2025-05-06
Start date
2025-11-05
Completion date
Unknown
Last updated
2026-03-23

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

Conditions

Bilharzia schistosomiasis

Interventions

None listed

Sponsors

IRCCS Sacro Cuore Don Calabria
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: (1) diagnosis of chronic schistosomiasis (>3 months after last potential exposure) according to site-specific diagnostic practice (2) signed informed consent (and assent for minors).

Exclusion criteria

Exclusion criteria: 1. age below 16 years; 2. exposure to praziquantel after the last potential exposure to schistosomes 3. acute infection, i.e. likely infection

Design outcomes

Primary

MeasureTime frame
Primary objective To determine the proportion of travelers and migrants diagnosed with chronic schistosomiasis according to site-specific diagnostic practice, who have active infection at presentation (as assessed and classified by composite reference standards integrating clinical, laboratory and diagnostic features, such as microscopy, PCR (where available), POC-CCA (where available), and serum CAA results). Endpoint: proportion of enrolled participants fulfilling the composite reference standards for active infection

Secondary

MeasureTime frame
To explore the accuracy and added value of serum CAA determination as test of cure 6 weeks after the WHO standard treatment regimen (40 mg/kg single dose praziquantel), compared to conventional (microscopy) and novel methods (PCR, POC-CCA) in sites where the latter would be available. Endpoint: number of participants with initial active infection who will be CAA negative at week 6 post-treatment compared to number of participants fulfilling the composite definition of clinical and parasitological cure, and to number of negative results by each other separate diagnostic method.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Apr 3, 2026