Hypoxic-Ischemic Encephalopathy Clinical Trial
— ULOOPOfficial title:
Umbilical Cord Abnormalities in the Prediction of Adverse Pregnancy Outcomes
NCT number | NCT05901688 |
Other study ID # | 001 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | October 3, 2023 |
Est. completion date | December 31, 2025 |
The objective of our study is to investigate the association of umbilical cord abnormalities with adverse pregnancy outcomes. The umbilical cord parameters that will be investigated as part of this study include the umbilical cord coiling index (UCI), umbilical cord (UC) diameter, umbilical vein (UV) diameter, UV flow velocity and the presence of nuchal cord. The UCI, UC, UV diameter & flow and presence of nuchal cord will be measured in routine unselected populations at 20-22 weeks and 35-37 weeks gestation during the study period. We will also measure the UC and UV diameter in a nested population of high-risk pregnancies attending our placental disorders clinic which have been deemed to be at risk of having adverse pregnancy outcomes. Primary objective: To investigate if prenatal assessment of UCI, UC, UV diameter & flow and presence of nuchal cord measured routinely in unselected screened populations at 20-22 weeks and 35-37 weeks' can provide an independent prediction of pregnancies that develop adverse pregnancy outcomes. Secondary objectives: To assess the correlation of UC and UV diameter measured by ultrasound scan and fetal magnetic resonance imaging in prediction of pregnancy outcome. To examine the association of these umbilical cord measurements and observations in a nested cohort of pregnancies in the high-risk placental disorders clinic.
Status | Recruiting |
Enrollment | 5000 |
Est. completion date | December 31, 2025 |
Est. primary completion date | July 3, 2025 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 16 Years and older |
Eligibility | Inclusion Criteria: 1. Singleton pregnancies. 2. Women booked at our unit prior to 20 weeks' gestation. Exclusion Criteria: 1. Multiple pregnancies. 2. Age < 16 years. 3. Those unable to provide consent. 4. Pregnancies with fetal abnormalities. |
Country | Name | City | State |
---|---|---|---|
United Kingdom | Medway NHS Foundation Trust | Gillingham | Kent |
Lead Sponsor | Collaborator |
---|---|
Medway NHS Foundation Trust |
United Kingdom,
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* Note: There are 25 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Delivery of small for gestational age (SGA) neonate | Birth weight below the 5th and 10th percentile | 2 years | |
Primary | Emergency CS for fetal distress | Caesarean section carried out for fetal heart rate abnormalities in labour | 2 years | |
Primary | Hypoxic ischaemic encephalopathy | Brain damage in neonates causes due to lack of oxygen and confirmed on ultrasound scan | 2 years | |
Primary | Stillbirth | Death of a fetuses between 24 weeks and before the birth of the baby | 2 years | |
Primary | Composite hypoxic morbidity | A composite outcome measures of any of the above outcome measures | 2 years | |
Secondary | Preterm delivery < 37 weeks | Spontaneous and iatrogenic preterm delivery | 2 years | |
Secondary | Development of preeclampsia | High blood pressure developing in pregnancy based on ISSHP criteria | 2 years | |
Secondary | Admission to neonatal intensive care unit | Admission to intensive or high-dependency care | 2 years |
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