Clinical Prognostic Score to Predict Relapse in VL

Recruiting Observational Study
Visceral Leishmaniasis
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
12 and older
Sex
Any
Study type
Observational
Participants needed
741 (estimated)
Sponsor
Institute of Tropical Medicine, Belgium · Other
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About This Trial
This prospective cohort study has the aim to develop a prognostic tool to predict relapse in patients suffering from visceral leishmaniasis (VL) from VL endemic regions in Ethiopia. Therefore, comprehensive clinical and laboratory characterization of all confirmed VL patients before and during treatment will be performed in order to identify the factors that determine prognosis of the patients. T…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * clinically or parasitologically confirmed VL Exclusion Criteria: * Age under 12 years * VL patients already on treatment for 3 days or more * Severe critical condition or other circumstances that make the study medically inadvisable * Unlikely to adhere to follow up visits d…
Contacts

Saskia van Henten, MD

+32(0)32476556

svanhenten@itg.be

CONTACT