Ondansetron to reduce neonatal opioid withdrawal severity a randomized clinical trial

J Perinatol. 2023 Mar;43(3):271-276. doi: 10.1038/s41372-022-01487-2. Epub 2022 Aug 27.

Abstract

Objective: To determine if treatment with a 5-HT3 antagonist (ondansetron) reduces need for opioid therapy in infants at risk for neonatal opioid withdrawal syndrome (NOWS).

Study design: A multicenter, randomized, placebo controlled, double blind clinical trial of ninety (90) infants. The intervention arms were intravenous ondansetron or placebo during labor followed by a daily dose of ondansetron or placebo in infants for five days.

Results: Twenty-two (49%) ondansetron-treated and 26 (63%) placebo-treated infants required pharmacologic treatment (p > 0.05). The Finnegan score was lower in the ondansetron-treated group (4.6 vs. 5.6, p = 0.02). A non-significant trend was noted for the duration of hospitalization. There was no difference in need for phenobarbital or clonidine therapy, or total dose of morphine in the first 15 days of NOWS treatment.

Conclusions: Ondansetron treatment reduced the severity of NOWS symptoms; and there was an indication that it could reduce the length of stay.

Clinical trial registration: Clinicaltrials.gov NCT01965704.

Publication types

  • Randomized Controlled Trial
  • Multicenter Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Analgesics, Opioid* / therapeutic use
  • Humans
  • Infant, Newborn
  • Morphine / adverse effects
  • Neonatal Abstinence Syndrome* / drug therapy
  • Ondansetron / therapeutic use
  • Phenobarbital / therapeutic use

Substances

  • Analgesics, Opioid
  • Ondansetron
  • Morphine
  • Phenobarbital

Associated data

  • ClinicalTrials.gov/NCT01965704