ArticlePloS one2025
Tropistry: A registry-based modular platform to improve care of neglected tropical diseases in nonendemic settings-Study protocol with two targeted conditions: acute schistosomiasis and cutaneous/mucocutaneous leishmaniasis.
Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Epidemiology of Imported Cutaneous Leishmaniasis: A Narrative Review.Microorganisms · 2026Review
- Inequitable access to medicines for neglected tropical diseases in Europe: health system vulnerabilities and a call for coordinated action.The Lancet regional health. Europe · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundNeglected tropical diseases (NTDs) are increasingly encountered in nonendemic settings due to migration, international travel, and global mobility. Their clinical management is often challenging: evidence from endemic regions is limited or not directly applicable, and healthcare providers are frequently unfamiliar with their diagnosis and treatment. Consequently, there is substantial heterogeneity in diagnostic workup, therapeutic choices, and follow-up strategies, which may affect patient outcomes and complicate guideline development. Given the sporadic presentation of these diseases across individual centers and the overall low caseload in nonendemic settings, conducting randomized controlled trials to define optimal strategies is largely unfeasible. To address these gaps, we designed Tropistry, a modular, multicenter registry that integrates harmonized data collection with embedded expert-informed clinical guidance.
methodsTropistry is an ambispective, multicenter registry planned for implementation across Belgian and European sites. Its modular structure will allow the sequential integration of disease-specific components, initially focusing on acute schistosomiasis and cutaneous/mucocutaneous leishmaniasis (CL/MCL), selected for their sporadic occurrence, clinical complexity, and lack of standardized management. Data will be collected through REDCap-based electronic case report forms aligned with up-to-date, evidence-based recommendations to ensure harmonized and comparable data collection. Embedded expert-informed guidance will support clinicians unfamiliar with these diseases, complemented by expedited access to ITM experts via TROPmail and aggregated feedback through an interactive R Shiny-based dashboard. A structured evaluation framework will assess feasibility, usability, data quality, user engagement, and treatment adherence to ensure the platform's utility and validity. EXPECTED IMPACT: By centralizing harmonized data on diagnostic and therapeutic practices, Tropistry aims to address critical knowledge gaps in managing NTDs in nonendemic settings. For the initial targeted conditions, it will help clarify optimal strategies, such as the combination of corticosteroids and praziquantel for acute schistosomiasis and best practices for therapy and follow-up in CL/MCL. Beyond data collection, Tropistry will provide embedded expert-informed guidance, interactive dashboards, and direct access to ITM experts to support clinicians and promote standardized care. Its modular design will enable expansion to other challenging NTDs, while the built-in evaluation framework ensures continuous assessment and optimization of feasibility, usability, and clinical utility. Ultimately, Tropistry seeks to strengthen collaboration between reference centers and non-specialized facilities and generate robust real-world evidence to inform clinical practice, guideline development, and future trials.
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