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Transplacental Aspirin Therapy for Early Onset Fetal Growth Restriction

Primary Purpose

Fetal Growth Restriction, Fetal Growth Retardation, Intrauterine Growth Restriction

Status
Withdrawn
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Aspirin
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fetal Growth Restriction focused on measuring Maternal Aspirin Therapy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Pregnant women at least 18 years old
  • Gestational age between 220/7 to 300/7 weeks
  • Fetal abdominal circumference < 10th percentile
  • Umbilical artery Doppler index elevation > 95th percentile
  • Forward umbilical artery end-diastolic flow
  • Able to understand purpose, risks/benefits, and voluntary nature of study participant

Exclusion Criteria:

  • Multiple pregnancy
  • Currently taking 81 mg aspirin
  • Maternal contraindication to aspirin treatment including allergy
  • Active vaginal bleeding
  • Presence of any physical fetal anomaly
  • Fetal viral infection if diagnosed by the appropriate diagnostic test
  • Fetal chromosomal abnormalities if diagnosed by invasive fetal testing
  • Need for imminent delivery

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    ASA Group

    SOC Group

    Arm Description

    Receives standard of care and intervention.

    Receives standard of care (SOC), only

    Outcomes

    Primary Outcome Measures

    Number of fetuses delivered for non-reassuring fetal status prior to 32+0 week's gestation
    To determine the frequency of delivery prior to 32+0 weeks' gestation for abnormal fetal surveillance parameters.

    Secondary Outcome Measures

    Change in UA Doppler index
    UA Doppler index is assessed at enrollment (baseline) and weekly. Qualitative changes in UA Doppler index are measured as presence, absence or reversal of end-diastolic velocity.
    Change in amniotic fluid index (AFI)
    Amniotic fluid index, measured with amniotic fluid volume [in centimeters (cm)] will be assessed at enrollment (baseline) and weekly. Oligohydramnios is an AFI ≤ 5 cm or a maximum vertical pocket (MVP) pocket ≤ 2 cm.
    Change in fetal heart rate decelerations
    Fetal heart rate decelerations [in milliseconds (ms)] is assessed at enrollment (baseline) and weekly to bi-weekly. Heart rate variability increases with gestational age. After 29 weeks gestation, 4.0 ms and 3.0 ms meet criteria for reduced or very low short-term variation (STV) respectively. Before 29 weeks gestation, an STV <3.5 ms is considered reduced and <2.6 ms as very low.
    Change in biophysical profile score
    Biophysical profile score is assessed at enrollment (baseline) and weekly to bi-weekly. The biophysical profile (BPP) combines a nonstress test (NST) with an ultrasound to evaluate a baby's heart rate, breathing, movements, muscle tone and amniotic fluid level. Each gives a score between 0 and 2 and are added up for a total maximum score of 10. A score of 8 or 10 is considered normal, while a score below 8 usually requires further evaluation or delivery of the baby.
    Gestational age at delivery
    Gestational age at delivery measured in weeks.
    Birthweight percentile at delivery
    Birthweight percentile will be assessed at the time of delivery.
    Placental size at delivery
    Placental size measured in grams at delivery.

    Full Information

    First Posted
    September 15, 2020
    Last Updated
    June 11, 2021
    Sponsor
    Johns Hopkins University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04557475
    Brief Title
    Transplacental Aspirin Therapy for Early Onset Fetal Growth Restriction
    Official Title
    A Randomized Trial of Transplacental Aspirin Therapy for Early Onset Fetal Growth
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2021
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    We are modifying this trial's protocol and will resubmit a new application at a later date.
    Study Start Date
    June 11, 2022 (Anticipated)
    Primary Completion Date
    June 11, 2023 (Anticipated)
    Study Completion Date
    June 11, 2023 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Johns Hopkins University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The purpose of this investigation is to evaluate the ability of maternal aspirin (ASA) therapy to prevent preterm birth for fetal indications prior to 32 weeks gestation in women with early onset Fetal Growth Restriction (FGR). Aspirin is a commonly used medication that blocks blood platelets from clumping. Aspirin crosses the placenta in a dose dependent mode. There is preliminary evidence in smaller studies that aspirin can block fetal platelet clumping and, therefore, slow down the progression of placental disease under specific circumstances. The optimal time for aspirin to work is when the fetus' placental dysfunction is still mild. The goal of this research study is to show if fetuses that receive aspirin through maternal intake at a dose shown to affect fetal platelet aggregation will be less likely to deliver before 32 weeks for fetal deterioration. The outcomes of patients that receive aspirin will be compared to women that receive standard FGR management but do not take any aspirin. The decision if a study participant receives aspirin or not will be randomly picked. Such a research study is called a randomized controlled trial.
    Detailed Description
    Early onset FGR requiring preterm delivery by 32 weeks gestation complicates 1-5% of pregnancies and is an important health problem. Over 60% of children have long-term health consequences after being delivered for early onset FGR. There is no prenatal treatment for fetal growth restriction. The current management of FGR consists of fetal surveillance to detect a decline in the baby's health and deliver when this can be safely done. In a large number of early onset FGR, premature delivery is required to prevent the fetus from becoming more compromised or even dying in the womb. Placental dysfunction leading to early onset FGR is characterized by changes to the blood vessels of the placenta, leading to a decline in the amount of blood flow to the placenta. The arteries that run in the umbilical cord of the fetus (umbilical arteries) are important for nutrient exchange between the fetal and placental circulation. Many fetuses with early onset FGR have elevated resistance in the blood vessels entering the placenta. This results in decreased blood flow in the umbilical artery (UA). The blood flow in the umbilical artery is evaluated by a specialized ultrasound technique called Doppler ultrasound. Doppler ultrasound of the umbilical arteries examines the blood flow to see if there is evidence of abnormal blood flow into the placenta. When the amount of blood flow at the end of every pulse decreases, it is classified as elevated UA blood flow resistance. When the blood flow briefly pauses at the end of each pulse, this is called absent end-diastolic velocity (AEDV) or UA AEDV. When the blood flow reverses at the end of each pulse, this is called reversed end-diastolic velocity (UA REDV). In fetuses with elevated UA blood flow, the placenta can usually supply enough nutrients and oxygen for at least 9 weeks. After that time, delivery is typically required. The worsening of blood flow to UA AEDV, or even UA REDV, increases the risk for fetal deterioration and preterm birth within the next 2-6 weeks. Approximately, 80% of early onset FGR fetuses progress to UA AEDV, or even UA REDV, and then require delivery by 32 weeks. There is no treatment that can stop this progression which is of critical importance in determining how much time is left for the fetus before delivery will be necessary.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Fetal Growth Restriction, Fetal Growth Retardation, Intrauterine Growth Restriction, Intrauterine Growth Retardation
    Keywords
    Maternal Aspirin Therapy

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Model Description
    Two Group Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    ASA Group
    Arm Type
    Experimental
    Arm Description
    Receives standard of care and intervention.
    Arm Title
    SOC Group
    Arm Type
    No Intervention
    Arm Description
    Receives standard of care (SOC), only
    Intervention Type
    Drug
    Intervention Name(s)
    Aspirin
    Other Intervention Name(s)
    acetylsalicylic acid (ASA)
    Intervention Description
    Two tablets daily with dinner
    Primary Outcome Measure Information:
    Title
    Number of fetuses delivered for non-reassuring fetal status prior to 32+0 week's gestation
    Description
    To determine the frequency of delivery prior to 32+0 weeks' gestation for abnormal fetal surveillance parameters.
    Time Frame
    From randomization until birth, up to 38 weeks gestation
    Secondary Outcome Measure Information:
    Title
    Change in UA Doppler index
    Description
    UA Doppler index is assessed at enrollment (baseline) and weekly. Qualitative changes in UA Doppler index are measured as presence, absence or reversal of end-diastolic velocity.
    Time Frame
    Baseline and weekly, up to 38 weeks gestation
    Title
    Change in amniotic fluid index (AFI)
    Description
    Amniotic fluid index, measured with amniotic fluid volume [in centimeters (cm)] will be assessed at enrollment (baseline) and weekly. Oligohydramnios is an AFI ≤ 5 cm or a maximum vertical pocket (MVP) pocket ≤ 2 cm.
    Time Frame
    Baseline and weekly, up to 38 weeks gestation
    Title
    Change in fetal heart rate decelerations
    Description
    Fetal heart rate decelerations [in milliseconds (ms)] is assessed at enrollment (baseline) and weekly to bi-weekly. Heart rate variability increases with gestational age. After 29 weeks gestation, 4.0 ms and 3.0 ms meet criteria for reduced or very low short-term variation (STV) respectively. Before 29 weeks gestation, an STV <3.5 ms is considered reduced and <2.6 ms as very low.
    Time Frame
    Baseline and weekly to bi-weekly, up to 38 weeks gestation
    Title
    Change in biophysical profile score
    Description
    Biophysical profile score is assessed at enrollment (baseline) and weekly to bi-weekly. The biophysical profile (BPP) combines a nonstress test (NST) with an ultrasound to evaluate a baby's heart rate, breathing, movements, muscle tone and amniotic fluid level. Each gives a score between 0 and 2 and are added up for a total maximum score of 10. A score of 8 or 10 is considered normal, while a score below 8 usually requires further evaluation or delivery of the baby.
    Time Frame
    Baseline and weekly to bi-weekly, up to 38 weeks gestation
    Title
    Gestational age at delivery
    Description
    Gestational age at delivery measured in weeks.
    Time Frame
    At time of birth, up to 38 weeks gestation
    Title
    Birthweight percentile at delivery
    Description
    Birthweight percentile will be assessed at the time of delivery.
    Time Frame
    At time of birth, up to 38 weeks gestation
    Title
    Placental size at delivery
    Description
    Placental size measured in grams at delivery.
    Time Frame
    At time of birth, up to 38 weeks gestation

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Pregnant women at least 18 years old Gestational age between 220/7 to 300/7 weeks Fetal abdominal circumference < 10th percentile Umbilical artery Doppler index elevation > 95th percentile Forward umbilical artery end-diastolic flow Able to understand purpose, risks/benefits, and voluntary nature of study participant Exclusion Criteria: Multiple pregnancy Currently taking 81 mg aspirin Maternal contraindication to aspirin treatment including allergy Active vaginal bleeding Presence of any physical fetal anomaly Fetal viral infection if diagnosed by the appropriate diagnostic test Fetal chromosomal abnormalities if diagnosed by invasive fetal testing Need for imminent delivery
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Ahmet A Baschat
    Organizational Affiliation
    Johns Hopkins University
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Ashi R Daftary, MD
    Organizational Affiliation
    Allegheny Health Network
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
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    Transplacental Aspirin Therapy for Early Onset Fetal Growth Restriction

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