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Withdrawn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
About this trial
This is an interventional treatment trial for Fetal Growth Restriction focused on measuring Maternal Aspirin Therapy
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
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
NCT ID
NCT04557475
First Posted
September 15, 2020
Last Updated
June 11, 2021
Sponsor
Johns Hopkins University
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
Citations:
PubMed Identifier
27223167
Citation
Khong TY, Mooney EE, Ariel I, Balmus NC, Boyd TK, Brundler MA, Derricott H, Evans MJ, Faye-Petersen OM, Gillan JE, Heazell AE, Heller DS, Jacques SM, Keating S, Kelehan P, Maes A, McKay EM, Morgan TK, Nikkels PG, Parks WT, Redline RW, Scheimberg I, Schoots MH, Sebire NJ, Timmer A, Turowski G, van der Voorn JP, van Lijnschoten I, Gordijn SJ. Sampling and Definitions of Placental Lesions: Amsterdam Placental Workshop Group Consensus Statement. Arch Pathol Lab Med. 2016 Jul;140(7):698-713. doi: 10.5858/arpa.2015-0225-CC. Epub 2016 May 25.
Results Reference
background
PubMed Identifier
9168580
Citation
Kingdom JC, Burrell SJ, Kaufmann P. Pathology and clinical implications of abnormal umbilical artery Doppler waveforms. Ultrasound Obstet Gynecol. 1997 Apr;9(4):271-86. doi: 10.1046/j.1469-0705.1997.09040271.x. No abstract available.
Results Reference
background
PubMed Identifier
2679101
Citation
Morrow RJ, Adamson SL, Bull SB, Ritchie JW. Effect of placental embolization on the umbilical arterial velocity waveform in fetal sheep. Am J Obstet Gynecol. 1989 Oct;161(4):1055-60. doi: 10.1016/0002-9378(89)90783-7.
Results Reference
background
PubMed Identifier
3966988
Citation
Giles WB, Trudinger BJ, Baird PJ. Fetal umbilical artery flow velocity waveforms and placental resistance: pathological correlation. Br J Obstet Gynaecol. 1985 Jan;92(1):31-8. doi: 10.1111/j.1471-0528.1985.tb01045.x.
Results Reference
background
PubMed Identifier
7856679
Citation
Jackson MR, Walsh AJ, Morrow RJ, Mullen JB, Lye SJ, Ritchie JW. Reduced placental villous tree elaboration in small-for-gestational-age pregnancies: relationship with umbilical artery Doppler waveforms. Am J Obstet Gynecol. 1995 Feb;172(2 Pt 1):518-25. doi: 10.1016/0002-9378(95)90566-9.
Results Reference
background
PubMed Identifier
30129125
Citation
Redline RW, Ravishankar S. Fetal vascular malperfusion, an update. APMIS. 2018 Jul;126(7):561-569. doi: 10.1111/apm.12849.
Results Reference
background
PubMed Identifier
2002988
Citation
Wilcox GR, Trudinger BJ. Fetal platelet consumption: a feature of placental insufficiency. Obstet Gynecol. 1991 Apr;77(4):616-21.
Results Reference
background
PubMed Identifier
12738160
Citation
Trudinger B, Song JZ, Wu ZH, Wang J. Placental insufficiency is characterized by platelet activation in the fetus. Obstet Gynecol. 2003 May;101(5 Pt 1):975-81. doi: 10.1016/s0029-7844(03)00173-x.
Results Reference
background
PubMed Identifier
9932551
Citation
Ohshige A, Yoshimura T, Maeda T, Ito M, Okamura H. Increased platelet-activating factor-acetylhydrolase activity in the umbilical venous plasma of growth-restricted fetuses. Obstet Gynecol. 1999 Feb;93(2):180-3. doi: 10.1016/s0029-7844(98)00407-4.
Results Reference
background
PubMed Identifier
9197883
Citation
Sciscione AC, Bessos H, Callan N, Blakemore K, Kickler T. Indicators of platelet turnover in thrombocytopenic infants. Br J Obstet Gynaecol. 1997 Jun;104(6):743-5. doi: 10.1111/j.1471-0528.1997.tb11990.x.
Results Reference
background
PubMed Identifier
10908756
Citation
Baschat AA, Gembruch U, Reiss I, Gortner L, Weiner CP, Harman CR. Absent umbilical artery end-diastolic velocity in growth-restricted fetuses: a risk factor for neonatal thrombocytopenia. Obstet Gynecol. 2000 Aug;96(2):162-6. doi: 10.1016/s0029-7844(00)00904-2.
Results Reference
background
PubMed Identifier
18634130
Citation
Turan OM, Turan S, Gungor S, Berg C, Moyano D, Gembruch U, Nicolaides KH, Harman CR, Baschat AA. Progression of Doppler abnormalities in intrauterine growth restriction. Ultrasound Obstet Gynecol. 2008 Aug;32(2):160-7. doi: 10.1002/uog.5386.
Results Reference
background
PubMed Identifier
24931475
Citation
Crimmins S, Desai A, Block-Abraham D, Berg C, Gembruch U, Baschat AA. A comparison of Doppler and biophysical findings between liveborn and stillborn growth-restricted fetuses. Am J Obstet Gynecol. 2014 Dec;211(6):669.e1-10. doi: 10.1016/j.ajog.2014.06.022. Epub 2014 Jun 12.
Results Reference
background
PubMed Identifier
29233550
Citation
Caradeux J, Martinez-Portilla RJ, Basuki TR, Kiserud T, Figueras F. Risk of fetal death in growth-restricted fetuses with umbilical and/or ductus venosus absent or reversed end-diastolic velocities before 34 weeks of gestation: a systematic review and meta-analysis. Am J Obstet Gynecol. 2018 Feb;218(2S):S774-S782.e21. doi: 10.1016/j.ajog.2017.11.566. Epub 2017 Dec 9.
Results Reference
background
PubMed Identifier
11876805
Citation
Ferrazzi E, Bozzo M, Rigano S, Bellotti M, Morabito A, Pardi G, Battaglia FC, Galan HL. Temporal sequence of abnormal Doppler changes in the peripheral and central circulatory systems of the severely growth-restricted fetus. Ultrasound Obstet Gynecol. 2002 Feb;19(2):140-6. doi: 10.1046/j.0960-7692.2002.00627.x.
Results Reference
background
PubMed Identifier
11844190
Citation
Hecher K, Bilardo CM, Stigter RH, Ville Y, Hackeloer BJ, Kok HJ, Senat MV, Visser GH. Monitoring of fetuses with intrauterine growth restriction: a longitudinal study. Ultrasound Obstet Gynecol. 2001 Dec;18(6):564-70. doi: 10.1046/j.0960-7692.2001.00590.x.
Results Reference
background
PubMed Identifier
11844191
Citation
Baschat AA, Gembruch U, Harman CR. The sequence of changes in Doppler and biophysical parameters as severe fetal growth restriction worsens. Ultrasound Obstet Gynecol. 2001 Dec;18(6):571-7. doi: 10.1046/j.0960-7692.2001.00591.x.
Results Reference
background
PubMed Identifier
16323151
Citation
Baschat AA, Galan HL, Bhide A, Berg C, Kush ML, Oepkes D, Thilaganathan B, Gembruch U, Harman CR. Doppler and biophysical assessment in growth restricted fetuses: distribution of test results. Ultrasound Obstet Gynecol. 2006 Jan;27(1):41-47. doi: 10.1002/uog.2657.
Results Reference
background
PubMed Identifier
25747582
Citation
Lees CC, Marlow N, van Wassenaer-Leemhuis A, Arabin B, Bilardo CM, Brezinka C, Calvert S, Derks JB, Diemert A, Duvekot JJ, Ferrazzi E, Frusca T, Ganzevoort W, Hecher K, Martinelli P, Ostermayer E, Papageorghiou AT, Schlembach D, Schneider KT, Thilaganathan B, Todros T, Valcamonico A, Visser GH, Wolf H; TRUFFLE study group. 2 year neurodevelopmental and intermediate perinatal outcomes in infants with very preterm fetal growth restriction (TRUFFLE): a randomised trial. Lancet. 2015 May 30;385(9983):2162-72. doi: 10.1016/S0140-6736(14)62049-3. Epub 2015 Mar 5. Erratum In: Lancet. 2015 May 30;385(9983):2152.
Results Reference
background
PubMed Identifier
30169244
Citation
Sharp A, Cornforth C, Jackson R, Harrold J, Turner MA, Kenny LC, Baker PN, Johnstone ED, Khalil A, von Dadelszen P, Papageorghiou AT, Alfirevic Z; STRIDER group. Maternal sildenafil for severe fetal growth restriction (STRIDER): a multicentre, randomised, placebo-controlled, double-blind trial. Lancet Child Adolesc Health. 2018 Feb;2(2):93-102. doi: 10.1016/S2352-4642(17)30173-6. Epub 2017 Dec 7. Erratum In: Lancet Child Adolesc Health. 2018 Feb;2(2):e2.
Results Reference
background
PubMed Identifier
3526896
Citation
Ylikorkala O, Makila UM, Kaapa P, Viinikka L. Maternal ingestion of acetylsalicylic acid inhibits fetal and neonatal prostacyclin and thromboxane in humans. Am J Obstet Gynecol. 1986 Aug;155(2):345-9. doi: 10.1016/0002-9378(86)90823-9.
Results Reference
background
PubMed Identifier
11048830
Citation
Parker CR Jr, Hauth JC, Goldenberg RL, Cooper RL, Dubard MB. Umbilical cord serum levels of thromboxane B2 in term infants of women who participated in a placebo-controlled trial of low-dose aspirin. J Matern Fetal Med. 2000 Jul-Aug;9(4):209-15. doi: 10.1002/1520-6661(200007/08)9:43.0.CO;2-S.
Results Reference
background
PubMed Identifier
3048102
Citation
Trudinger BJ, Cook CM, Thompson RS, Giles WB, Connelly A. Low-dose aspirin therapy improves fetal weight in umbilical placental insufficiency. Am J Obstet Gynecol. 1988 Sep;159(3):681-5. doi: 10.1016/s0002-9378(88)80034-6.
Results Reference
background
PubMed Identifier
8717556
Citation
Newnham JP, Godfrey M, Walters BJ, Phillips J, Evans SF. Low dose aspirin for the treatment of fetal growth restriction: a randomized controlled trial. Aust N Z J Obstet Gynaecol. 1995 Nov;35(4):370-4. doi: 10.1111/j.1479-828x.1995.tb02144.x.
Results Reference
background
PubMed Identifier
10428519
Citation
McCowan LM, Harding J, Roberts A, Barker S, Ford C, Stewart A. Administration of low-dose aspirin to mothers with small for gestational age fetuses and abnormal umbilical Doppler studies to increase birthweight: a randomised double-blind controlled trial. Br J Obstet Gynaecol. 1999 Jul;106(7):647-51. doi: 10.1111/j.1471-0528.1999.tb08362.x.
Results Reference
background
PubMed Identifier
28670938
Citation
Ali MK, Abbas AM, Yosef AH, Bahloul M. The effect of low-dose aspirin on fetal weight of idiopathic asymmetrically intrauterine growth restricted fetuses with abnormal umbilical artery Doppler indices: a randomized clinical trial. J Matern Fetal Neonatal Med. 2018 Oct;31(19):2611-2616. doi: 10.1080/14767058.2017.1350160. Epub 2017 Jul 11.
Results Reference
background
PubMed Identifier
26909664
Citation
Gordijn SJ, Beune IM, Thilaganathan B, Papageorghiou A, Baschat AA, Baker PN, Silver RM, Wynia K, Ganzevoort W. Consensus definition of fetal growth restriction: a Delphi procedure. Ultrasound Obstet Gynecol. 2016 Sep;48(3):333-9. doi: 10.1002/uog.15884.
Results Reference
background
PubMed Identifier
17267821
Citation
Baschat AA, Cosmi E, Bilardo CM, Wolf H, Berg C, Rigano S, Germer U, Moyano D, Turan S, Hartung J, Bhide A, Muller T, Bower S, Nicolaides KH, Thilaganathan B, Gembruch U, Ferrazzi E, Hecher K, Galan HL, Harman CR. Predictors of neonatal outcome in early-onset placental dysfunction. Obstet Gynecol. 2007 Feb;109(2 Pt 1):253-61. doi: 10.1097/01.AOG.0000253215.79121.75.
Results Reference
background
PubMed Identifier
31499415
Citation
Sharp A, Jackson R, Cornforth C, Harrold J, Turner MA, Kenny L, Baker PN, Johnstone ED, Khalil A, von Dadelszen P, Papageorghiou AT, Alfirevic Z. A prediction model for short-term neonatal outcomes in severe early-onset fetal growth restriction. Eur J Obstet Gynecol Reprod Biol. 2019 Oct;241:109-118. doi: 10.1016/j.ejogrb.2019.08.007. Epub 2019 Aug 16.
Results Reference
background
PubMed Identifier
21520312
Citation
Baschat AA. Neurodevelopment following fetal growth restriction and its relationship with antepartum parameters of placental dysfunction. Ultrasound Obstet Gynecol. 2011 May;37(5):501-14. doi: 10.1002/uog.9008.
Results Reference
background
PubMed Identifier
12015543
Citation
Pardey J, Moulden M, Redman CW. A computer system for the numerical analysis of nonstress tests. Am J Obstet Gynecol. 2002 May;186(5):1095-103. doi: 10.1067/mob.2002.122447.
Results Reference
background
PubMed Identifier
23065842
Citation
Baschat AA, Kush M, Berg C, Gembruch U, Nicolaides KH, Harman CR, Turan OM. Hematologic profile of neonates with growth restriction is associated with rate and degree of prenatal Doppler deterioration. Ultrasound Obstet Gynecol. 2013 Jan;41(1):66-72. doi: 10.1002/uog.12322. Epub 2012 Dec 14.
Results Reference
background
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Transplacental Aspirin Therapy for Early Onset Fetal Growth Restriction
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