Observational Study of the Safety of Intravenous Artesunate Treatment of Pregnant Women and Their Infants

Recruiting Observational Study
Pregnancy Malaria
No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
15 – 100
Sex
Female
Study type
Observational
Participants needed
25 (estimated)
Sponsor
Amivas Inc. · Industry
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About This Trial

This study is a prospective observational study in which a female patient who received IV Artesunate while pregnant can volunteer to provide information about her pregnancy and the outcome of her pregnancy. Information will be collected from patient's provider, the patient's obstetrician, the child's pediatrician, or other relevant healthcare provider.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patient received IV Artesunate * Patient was pregnant while receiving IV Artesunate * Patient was at least 15 years of age * Patient or legal guardian/representative gave consent for the study and to collect data from her physicians Exclusion Criteria • None
Contacts

Katrina Riggs

3017622609

kriggs@fastttrackresearch.com

CONTACT