SCRIPT: Sickle Cell Risk in Pregnancy Tool
At a glance
Conditions
Where it's being run
3 sites across 3 statesStudy leadership
- A. Kinga Malinowski, MD, MSc · PRINCIPAL_INVESTIGATOR · MOUNT SINAI HOSPITAL
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.
Inclusion
Exclusion
What this trial measures
- Presence of Adverse Pregnancy OutcomeDuring pregnancy (until delivery of infant, up to 42 weeks of gestation)
Yes, if any of the following events first noted during the pregnancy within the study period: acute anemia (yes, no), cardiac complication (yes, no), pulmonary complication (yes, no), hepatobiliary complication (yes, no), MSK complication (yes, no), splenic complication (yes, no), neurologic complication (yes, no), renal complication (yes, no); multi-organ failure (yes, no), venous thromboembolism (yes, no), vaso-occlusive event with admission (yes, no), red cell transfusion (yes, no), maternal mortality (yes, no), hypertensive disorder of pregnancy (yes, no), preterm birth (yes, no), small for gestational age (yes, no), or perinatal mortality (yes, no); defined based on published classifications.