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Completed

NCT Number: NCT02851303

Morphine Versus Methadone for Opiate Exposed Infants With Neonatal Abstinence Syndrome

This study investigates the use of methadone versus morphine wean for the treatment of neonatal abstinence syndrome for infants exposed to opioids in utero. Half of infants who require pharmacotherapy for NAS will receive a methadone wean, and half will receive a morphine wean. Length of hospital stay, length of treatment and parent satisfaction will be studied.

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Key information

Age range

0 hour–12 hour

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

University of New Mexico Health Sciences Center

Albuquerque, New Mexico, 87106, United States

About this study

Neonates exposed to opiates in utero can develop a constellation of withdrawal symptoms known as neonatal abstinence syndrome (NAS). Infants with NAS are at risk for multiple medical complications including failure to thrive and seizures, they often require prolonged hospital stays and account for significant health care costs. At University of New Mexico, infants exposed to methadone or heroin in utero who develop NAS requiring pharmacologic treatment undergo a treatment wean with methadone, whereas infants exposed to buprenorphine undergo a wean with morphine. However, morphine is used frequently to treat neonatal abstinence syndrome among methadone-exposed infants throughout the US, and optimal pharmacologic treatment for NAS remains unknown. Anecdotal evidence at the investigators institution suggests that infants treated with morphine have shorter hospital stays compared to infants treated with methadone. Investigators propose a pilot randomized controlled trial to evaluate morphine vs methadone treatment of infants with in-utero methadone or heroin exposure. Specifically, length of treatment, need for additional medication to treat withdrawal, and length of hospital stay will be compared.

When women are admitted to Labor and Delivery and/or up to 12 hours postpartum, research staff will approach patients about study enrollment. Participants will be approached for study enrollment if medication list on admission includes methadone, if participants self-report methadone use prenatally, and/ or if urine drug screen is positive for methadone or opiates on admission. If women choose to enroll in the study, and their infants require treatment for NAS, their infants will be randomized and assigned a study number for treatment using the methadone or morphine protocols at the time treatment is required.

All infants will be monitored for signs of withdrawal using the standard UNM NAS scoring protocol. Standard of care at UNM is to treat infants exposed to opioids in-utero with methadone if they require pharmacologic therapy for NAS, therefore treatment will not be withheld if they choose not to enroll in the study. Standard of care is also to obtain a urine drug screen on all infants with reported exposure to opiates in pregnancy. Enrolled patients will thus undergo routine urine drug screening. The only difference from standard care with regards to the study protocol is the treatment of half of the methadone or heroin exposed infants with morphine. The morphine protocol is proven for safety and efficacy currently in buprenorphine exposed infants. Once randomized, infants will continue on the protocol until discharge. At discharge, parents will complete a patient satisfaction survey.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Born at University of New Mexico Hospital
  • Greater than 34 weeks gestation
  • Primary in-utero drug exposure was opioids other than buprenorphine
  • Maternal or infant urine drug screen positive for methadone and/or opioids on admission

Exclusion criteria

  • Born prior to 34 weeks
  • Neonatal intensive care unit admission
  • Serious medical comorbidities
  • Primary substance exposure in-utero was buprenorphine, or was not opioids

Treatment and study plan

Morphine

Drug

Morphine wean protocol as described in arm description

Methadone

Drug

Methadone wean protocol as described in arm description

Primary outcomes

  1. Length of Hospital Stay

    Time frame: assessed at hospital discharge, approximately 7-30 days

    Number of days in hospital after birth

Secondary outcomes

  1. Length of Treatment

    Time frame: assessed at hospital discharge, approximately 7-30 days

  2. Need for Additional Agent to Treat Withdrawal, Determined by Chart Review of Medication Administration Record of Administered Medications for Withdrawal Treatment (Example: Clonidine or Phenobarbital)

    Time frame: assessed at hospital discharge, approximately 7-30 days

    clonidine

  3. Need for Feeding Assistance, Determined by Chart Review of Discharge Summary, Specifically Evaluating for Need for Nasogastric Tube Placement or Peripheral Parenteral Nutrition.

    Time frame: assessed at hospital discharge, approximately 7-30 days

  4. Need for NICU Transfer, as Determined by Chart Review of Discharge Summary.

    Time frame: assessed at hospital discharge, approximately 7-30 days

  5. Breastfeeding Initiation and Continuation at Hospital Discharge

    Time frame: assessed at hospital discharge, approximately 7-30 days

    Assessed through chart review of discharge summary documentation of method of infant feeding at time of discharge

  6. Total Morphine Equivalent Dose Received

    Time frame: assessed at hospital discharge, approximately 7-30 days

Sponsors and collaborators

Lead sponsor

University of New Mexico

Other

Registry information

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
Aug 1, 2016
Registry last updated
May 24, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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