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  • HP:0001622: Premature birth
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    HP:0001622: Premature birth

    Developed by Shray Alag, The Harker School
    Sections: Correlations, Clinical Trials, and HPO

    Correlations computed by analyzing all clinical trials.

    Navigate: Clinical Trials and HPO


    Correlated Drug Terms (4)


    Name (Synonyms) Correlation
    drug2803 Randomized to Delayed Cord Clamping at birth Wiki 1.00
    drug2804 Randomized to Umbilical Cord Milking at birth Wiki 1.00
    drug1540 Hydroxychloroquine Sulfate + Azithromycin Wiki 1.00
    Name (Synonyms) Correlation
    drug1538 Hydroxychloroquine Sulfate Wiki 0.29

    Correlated MeSH Terms (2)


    Name (Synonyms) Correlation
    D000013 Congenital Abnormalities NIH 0.71
    D047928 Premature Birth NIH 0.58

    Correlated HPO Terms (0)


    Name (Synonyms) Correlation

    Clinical Trials

    Navigate: Correlations   HPO

    There is one clinical trial.


    1 Two Year Developmental Follow-up for Premature Infants Receiving Milking or Delayed Cord Clamping: PREMOD2

    An extension of the PREMOD2 trial, the PREMOD2 Follow-Up trial will evaluate the neurodevelopmental outcomes at 22-26 months corrected age of preterm children who received UCM or DCC. This prospective multi-national randomized controlled trial (RCT) is a two-arm parallel non-inferiority design of two alternative approaches of treatment.

    NCT03476980
    Conditions
    1. Neurodevelopmental Abnormality
    Interventions
    1. Procedure: Randomized to Umbilical Cord Milking at birth
    2. Procedure: Randomized to Delayed Cord Clamping at birth
    MeSH:Premature Birth Congenital Abnormalities
    HPO:Premature birth

    Primary Outcomes

    Description: Bayley Scales of Infant Development (BSID), 3rd or 4th Ed. Composite Score (cognitive 55-145, language 45-155, motor 45-155; higher scores are better)

    Measure: Developmental Outcome

    Time: 22-26 months corrected gestational age (CGA). All assessments may be extended to 42 months CGA due to Covid-19 pandemic.

    Secondary Outcomes

    Description: Defined having at least one of the following: a cognitive score <70, GMFCS greater or equal 2, blindness (vision <20/200), or hearing impairment interfering with the ability to communicate with amplification.

    Measure: Moderate/Severe Neurodevelopmental Impairment

    Time: 22-26 months corrected gestational age

    Description: Defined having at least one of the following: a cognitive score 70-84, GMFCS =1, unilateral blindness (vision <20/200 in only one eye), or hearing impairment which does not interfere with the ability to communicate.

    Measure: Mild Neurodevelopmental Impairment

    Time: 22-26 months corrected gestational age

    Description: The GMFCS is a validated system used to describe the severity of motor dysfunction. Scale measured from Level 0-5 with Level 0 being normal and Level 5 being the worst score. Measures ability to walk, sit, head control, voluntary movements and postures.

    Measure: Gross Motor Function Classification System Scale (GMFCS)

    Time: 22-26 months corrected gestational age

    Description: Classified as None, Mild, Moderate or Severe based on GMFCS score; No CP = GMFCS Level 0, Mild CP = GMFCS Level 1, Moderate CP = GMFCS Levels 2-3, Severe CP = GMFCS Levels 4-5

    Measure: Cerebral Palsy (CP)

    Time: 22-26 months corrected gestational age

    Description: Each domain is scored from 0 to 60, the higher score is better.

    Measure: Developmental Outcomes assessed by Ages & Stages Questionnaire, 3rd ed. (ASQ-3) five domains: Communication, Gross motor, Fine motor, Problem solving and Personal-social in infants born between 23-32+6 weeks GA who received UCM or DCC.

    Time: 22-26 months corrected gestational age

    Description: BSID Cognitive, Language & Motor composite scores (cognitive 55-145, language 45-155, motor 45-155; higher scores are better) in infants 23-27 weeks GA and 28-32+6 weeks GA.

    Measure: Developmental Outcomes in infants born at 23 -27 and 28-32 weeks GA who received UCM or DCC

    Time: 22-26 months corrected gestational age

    Description: ASQ-3 scores (0 to 60, the higher score is better) in infants 23-27 weeks GA and 28-32+6 weeks GA.

    Measure: Developmental Outcomes in infants born at 23 -27 and 28-32 weeks GA who received UCM or DCC

    Time: 22-26 months corrected gestational age

    Description: Mild, moderate or severe impairment

    Measure: Compare levels of developmental impairment as assessed by BSID-3 or 4 versus the ASQ-3 screening tool.

    Time: 22-26 months corrected gestational age

    Description: Any IVH grade from 1 to grade 4, higher grade is worse

    Measure: Any grade intraventricular hemorrhage (IVH) in premature newborns 23 - 32+6 weeks GA who received UCM or DCC by mode of delivery (C-Section vs vaginal delivery)

    Time: From birth through hospital discharge, up to 6 months corrected gestational age (CGA)

    Description: Death

    Measure: Death in premature newborns 23 - 32+6 weeks GA who received UCM or DCC by mode of delivery (C-Section vs vaginal delivery)

    Time: From birth through hospital discharge, up to 6 months corrected gestational age (CGA)

    Description: BSID Cognitive, Language & Motor composite scores (cognitive 55-145, language 45-155, motor 45-155; higher scores are better)

    Measure: Compare neurodevelopmental outcomes from BSID assessments in newborns 23-32 weeks GA delivered by C-Section with those born by vaginal delivery receiving UCM or DCC.

    Time: 22-26 months corrected gestational age

    Description: ASQ-3 scores (0 to 60, the higher score is better).

    Measure: Compare neurodevelopmental outcomes from ASQ assessments in newborns 23-32 weeks GA delivered by C-Section with those born by vaginal delivery receiving UCM or DCC.

    Time: 22-26 months corrected gestational age

    Other Outcomes

    Description: Any grade IVH, from 1 to 4 (higher is worse)

    Measure: Exploratory, hypothesis-generating

    Time: From birth through hospital discharge, up to 6 months corrected gestational age (CGA)

    Description: Hemoglobin or Hematocrit at 4 hours of age

    Measure: Exploratory, hypothesis-generating

    Time: 4 hours of life +/- 2 hours

    Description: Delivery room interventions received: positive pressure ventilation, continuous positive airway pressure, intubation, chest compressions and medications

    Measure: Exploratory, hypothesis-generating

    Time: In the first 10 minutes of life

    Description: Blood pressures in the first 24 hours of life: on admission, 6, 12, 18 and 24 hours of life

    Measure: Exploratory, hypothesis-generating

    Time: In the first 24 hours of life

    HPO Nodes


    Reports

    Data processed on September 26, 2020.

    An HTML report was created for each of the unique drugs, MeSH, and HPO terms associated with COVID-19 clinical trials. Each report contains a list of either the drug, the MeSH terms, or the HPO terms. All of the terms in a category are displayed on the left-hand side of the report to enable easy navigation, and the reports contain a list of correlated drugs, MeSH, and HPO terms. Further, all reports contain the details of the clinical trials in which the term is referenced. Every clinical trial report shows the mapped HPO and MeSH terms, which are also hyperlinked. Related HPO terms, with their associated genes, protein mutations, and SNPs are also referenced in the report.

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