Thromboelastography (TEG) In the Intrauterine Growth Restriction (IUGR) Neonatal Population by Gestational Age
Withdrawn before enrolling
Conditions studied: Intrauterine Growth Restriction
In brief
The investigators aim to improve the understanding of TEG in this population in an effort to improve outcomes in a population at high risk in both the presence and absence of blood product transfusions.
Key facts
- Study ID
- NCT04907578
- Run by
- University of Pittsburgh
- People needed
- 0
- Starts
- 2021-08-12
- Expected to finish
- 2021-08-12
- Last updated by the study team
- 2021-08-18
Who can join
Age: any. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Participants included for medical record data and blood sample collection will be:
- Neonates diagnosed with intrauterine growth restriction, defined as a weight below the estimated 10th percentile and accordingly identified as such in any peripartum evaluation AND
- May have additional comorbidities AND
- Full term IUGR neonates will be have a gestational age of 37 weeks or greater OR
- Preterm IUGR neonates will have a gestational age less than 37 weeks OR
- Preterm IUGR neonates will have a gestational age less than 37 weeks
- Participants included for medical record review data collection ONLY will be:
- Mothers of eligible neonates
You may not qualify if…
- Constitutionally (familial) low birth weight, i.e. small for gestational age, babies OR
- Born to women with life threatening coexisting morbidities (this may include severe pre-eclampsia, diabetes or suspected infections including HIV or herpes) OR
- Neonates with an abnormal delivery or perinatal course including:
- Fetal demise, death in the first week after birth, neonatal encephalopathy, meconium aspiration, and physical birth injuries (fractures and brachial plexus injuries)
Where it is running
- UPMC Magee-Womens Hospital — Pittsburgh, Pennsylvania, United States
Full record on ClinicalTrials.gov
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