Improving Outcomes in Neonatal Abstinence Syndrome



Status:Active, not recruiting
Conditions:Psychiatric
Therapuetic Areas:Psychiatry / Psychology
Healthy:No
Age Range:Any
Updated:9/14/2018
Start Date:September 2013
End Date:December 2018

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1: SPECIFIC AIM I: To compare treatment options for neonatal abstinence syndrome (NAS) due to
in-utero narcotic exposure. One hundred eighty four full-term infants with a diagnosis of NAS
requiring medications will be studied. Infants will be randomized to receive either morphine
or methadone. It is hypothesized that morphine treated infants will do better and require
fewer days in the hospital compared to methadone treated infants.

2. SPECIFIC AIM II: To evaluate the effects of NAS treatment on long-term neurodevelopmental
outcome. Infants will be evaluated with development testing at 18 months of age. It is
hypothesized that morphine treated infants will have better neurodevelopmental outcomes. It
is also hypothesized that neurobehavioral abnormalities identified at two weeks of age will
correlate with neurodevelopmental impairment at 18 months.

3: SPECIFIC AIM III: To determine if common genetic variations in the genes involving
narcotic action contribute to the severity of NAS. A DNA sample will be obtained from all
infants and analyzed for differences in 3 key genes. This will then be correlated with
short-term and long-term outcomes.

1: SPECIFIC AIM I: To compare the short term efficacy of morphine and methadone for the
treatment of NAS. One hundred eighty four term infants with a diagnosis of NAS requiring
pharmacotherapy will be studied. Infants born to mothers receiving adequate prenatal care and
maintained on opioid agonist medication during pregnancy will be eligible. Infants will be
randomized to receive either neonatal morphine solution or methadone in a double blind,
double dummy design. It is hypothesized that morphine treated infants will require
significantly fewer days in the hospital compared to methadone treated infants. While the
primary outcome is the total length of initial hospital stay (LOS), total LOS related to NAS,
total duration of medical treatment for NAS, the need for a second drug to control symptoms,
and infant growth will also be evaluated as important secondary outcomes by medication group
assignment.

2. SPECIFIC AIM II: To evaluate the effects of NAS treatment on long-term neurodevelopmental
outcome. Infants in both treatment groups will be evaluated at 18 months of age using the
Bayley III Scales of Infant Development. It is hypothesized that morphine treated infants
will have better neurodevelopmental outcomes at 18 months compared to methadone treated
infants. It is also hypothesized that neurobehavioral abnormalities (from either treatment
group) identified at two weeks of age using the NICU Network Neurobehavioral Scale (NNNS)
will correlate with neurodevelopmental impairment detected with the Bayley III. Early
identification of infants at highest risk for impaired development will facilitate
therapeutic interventions to improve outcome and decrease resource utilization.

3: SPECIFIC AIM III: To determine if single nucleotide polymorphisms (SNPs) in genes
controlling opioid pharmacodynamics contribute to the severity of NAS. SNP genotyping from
cord blood or buccal swabs will be obtained from all infants and correlated with short term
outcomes (Aim 1) and neurodevelopment assessments (Aim 2) to confirm that genetic variation
plays a major role in the severity and outcome of infants with NAS.

Inclusion criteria:

1. Mother receiving methadone or buprenorphine (BPH) from a licensed physician or drug
treatment program, or an opioid prescribed by a licensed health care worker for
treatment of chronic pain.

2. Need for treatment of NAS by Finnegan Scoring criteria

3. Gestational age >37 weeks at birth defined by best obstetrical estimate

4. Medically stable in the opinion of the Attending Physician

5. Mother receiving "adequate" or "intermediate" prenatal care from a qualified physician
or midwife as defined by the Prenatal Care Adequacy Index

6. Singleton pregnancy

7. Mother able to provide informed consent

8. Infant able to take oral medications

Exclusion criteria:

1. Gestation <37 weeks at entry defined by best obstetrical estimate

2. Major congenital abnormalities including genetic syndromes

3. Serious medical illness such as sepsis, asphyxia, seizures, or respiratory failure

4. Mother abusing alcohol during pregnancy (average of 3 or more drinks per week in the
last 30 days)

5. Multiple gestations

6. Mother received "inadequate" prenatal care as defined by the Prenatal Care Adequacy
Index.
We found this trial at
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Boston, Massachusetts 02118
Principal Investigator: Michael Silverstein, MD
Phone: 617-414-3690
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800 Washington St
Boston, Massachusetts 02111
(617) 636-5000
Principal Investigator: Jonathan Davis, MD
Phone: 617-636-5322
Tufts Medical Center Tufts Medical Center is an internationally-respected academic medical center – a teaching...
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Jacksonville, Florida
Phone: 904-244-4242
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22 Bramhall St
Portland, Maine 04102
(207) 662-0111
Principal Investigator: Peter Marro, MD
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2201 West End Ave
Nashville, Tennessee 37232
(615) 322-7311
Principal Investigator: Barbara Engelhardt, MD
Phone: 615-322-3475
Vanderbilt University Vanderbilt offers undergraduate programs in the liberal arts and sciences, engineering, music, education...
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200 Lothrop St
Pittsburgh, Pennsylvania 15213
Principal Investigator: Debra L Bogen, MD
Phone: 412-692-6932
University of Pittsburgh Medical Center UPMC is one of the leading nonprofit health systems in...
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101 Dudley St
Providence, Rhode Island 02905
(401) 274-1100
Principal Investigator: Barry Lester, PhD
Phone: 401-453-7640
Women and Infants Hospital of Rhode Island Women & Infants Hospital of Rhode Island, a...
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759 Chestnut Street
Springfield, Massachusetts 01199
(413) 794 - 0000
Principal Investigator: Jeffrey Shenberger, MD
Phone: 413-794-5370
Baystate Medical Center Baystate Medical Center (BMC), in Springfield, Massachusetts, is an academic, research, and...
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