Pregnancy Clinical Trial
Official title:
Longitudinal Study of Intra-Uterine Growth Restriction (IUGR)
NCT number | NCT02382601 |
Other study ID # | 14-1360 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | April 2015 |
Est. completion date | December 2025 |
Verified date | May 2024 |
Source | University of Colorado, Denver |
Contact | Emma Peek, BS |
emma.peek[@]cuanschutz.edu | |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The investigation will employ a longitudinal approach in which every fetus diagnosed to be SGA (Small for Gestational Age ) will be studied at frequent intervals with sophisticated imaging techniques to assess subtle physiologic changes in the brain, heart, and placenta over time. These findings will be correlated with neurological and cardiovascular function in the newborn and early childhood. This research initiative should yield diagnostic and therapeutic templates that will improve the quality of life of IUGR babies in addition to providing important information that will better inform current diagnostic practices.
Status | Recruiting |
Enrollment | 200 |
Est. completion date | December 2025 |
Est. primary completion date | December 2025 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 45 Years |
Eligibility | Inclusion Criteria: - Patients with diagnosed SGA by an ultrasound estimated fetal weight (EFW) of less than the 10th percentile or a fetal abdominal circumference of less than the 5th percentile will be included in the study at the time of their first examination. Exclusion Criteria: - Patients < 18 years of age, and chromosomal anomalies as identified by regular aneuploidy screening. |
Country | Name | City | State |
---|---|---|---|
United States | University of Colorado Denver Anschutz Medical Campus | Aurora | Colorado |
Lead Sponsor | Collaborator |
---|---|
University of Colorado, Denver | The Perelman Family Foundation |
United States,
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* Note: There are 27 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Characterize the sequence of neurological and cardiovascular events defining early and late IUGR pathogenesis, respectively | Using ultrasound and MRI to identify changes in the fetal vasculature, and fetal brain as early and late IUGR progress. | Every two weeks from the time of IUGR diagnosis or first visit | |
Secondary | Correlate in utero adaptations in early and late IUGR, to infant and early childhood neurodevelopment | Assess neurodevelopment with a series of tests (PSOM, Bayleys III, Mullen's Scale of Early Learning, Developmental Profile-3, Child Behavior Checklist) and correlate neurological in utero findings to neurodevelopment outcomes after birth. | Baseline (Day 0), 40-44 weeks gestational age (post-birth), 6 months, 1-7 years | |
Secondary | Correlate in utero adaptations in early and late IUGR, to infant and early childhood cardiovascular outcomes | Assess cardiovascular health via heart ultrasound after birth | Baseline (Day 0), 40-44 weeks gestational age (post-birth), 6 months, 1-7 years | |
Secondary | Correlate in utero adaptations in early and late IUGR, to infant and early childhood metabolic outcomes | Correlate IUGR severity to metabolic outcomes as assessed by body composition (pea pod and bod pod with a pediatric attachment), anthropometrics, and a diet questionnaire after birth. | Baseline (Day 0), 40-44 weeks gestational age (post-birth), 6 months, 1-7 years | |
Secondary | Compare early IUGR, late IUGR and SGA infant and early childhood outcomes | Using the tests describe above compare the outcomes of each group after birth. | Baseline (Day 0), 40-44 weeks gestational age (post-birth), 6 months, 1-7 years |
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