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

Description

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.

Conditions

Pregnancy, Malaria

Study Overview

Study Details

Study overview

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.

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

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

Condition
Pregnancy
Intervention / Treatment

-

Contacts and Locations

Piscataway

4C Pharma Solutions, Piscataway, New Jersey, United States, 08854

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility 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

Ages Eligible for Study

15 Years to 100 Years

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

Amivas (US), LLC,

Bryan Smith, MD, PRINCIPAL_INVESTIGATOR, Amivas (US), LLC

Study Record Dates

2029-07-01