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.
Eligibility criteria
Qualifiers
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
Disqualifiers
None
Trial design
Treatments tested in this trial
- Not listed
Trial groups
No trial groups listed
Sponsors and collaborators
Source ClinicalTrials.gov