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Assessment of Infection Activity in Travelers and Migrants Diagnosed With Chronic Schistosomiasis
Sponsor: IRCCS Sacro Cuore Don Calabria di Negrar
Summary
The primary objective of this clinical investigation is to determine the percentage of travelers and migrants diagnosed with chronic schistosomiasis according to site-specific diagnostic practice who have active infection at the time of evaluation (as assessed and classified by composite reference standards that integrate clinical, laboratory, and diagnostic features, such as microscopy, PCR (where available), POC-CCA (where available), and serum CAA results). All subjects with chronic schistosomiasis according to site-specific diagnostic practice will have a standardized baseline clinical and laboratory evaluation at the time of evaluation that will include blood sampling for hematology, schistosome serology available at each site, and schistosome PCR where available; urine sampling for microscopy, determination of hematuria as an indirect marker of morbidity for schistosomiasis, and Schistosome PCR (where available), and urine strip testing POC-CCA (where available); and stool sampling for microscopy and PCR, where available, and fecal occult blood as indirect markers of schistosomiasis morbidity. Composite reference standards will be used to assess and classify the activity of the infection. Organ-specific ultrasound and other tests will be left to the physician's decision, but results will also be collected. Serum (at least 1 ml remaining from routine diagnostics) will be sent to LUMC, the Netherlands, where CAA will be determined with the UCP-LF CAA test designed for routine use. Participants will be asked to sign an additional consent form, which is optional and not precluding enrollment in the study, to allow the remaining serum to be stored at LUMC for 15 years, to allow secondary research.
Official title: Assessment of Infection Activity in Travelers and Migrants Diagnosed With Chronic Schistosomiasis: a Multicentric Prospective Cohort Study
Key Details
Gender
All
Age Range
5 Years - Any
Study Type
INTERVENTIONAL
Enrollment
278
Start Date
2024-06-28
Completion Date
2027-01
Last Updated
2025-04-20
Healthy Volunteers
No
Conditions
Interventions
UCP-LF CAA assay
dry LF-CAA, or CAA
Locations (8)
Institute of Tropical Medicine (ITM)
Antwerp, Belgium
Universitätsklinikum Hamburg-Eppendorf
Hamburg, Germany
IRCCS Policlinico Sant'Orsola
Bologna, BO, Italy
IRCCS Sacro Cuore Don Calabria
Negrar, VR, Italy
AOU Careggi
Florence, Italy
Medical Microbiology & Infectious Diseases, Erasmus MC
Rotterdam, Netherlands
Tropical Medicine Unit of Hospital de Poniente
Almería, Spain
Vall d'Hebron University Hospital
Barcelona, Spain