Vitality in Infants Via Azithromycin for Neonates Trial

21-34232

Nearly half of child deaths occur during the neonatal period, and 80% of those occur in babies with low birthweight. Although tremendous progress has been made towards reducing under-five mortality globally, declines in neonatal mortality lag behind those observed in older children. Low birthweight babies are at increased risk of poor outcomes compared to those who are term-appropriate for gestational age, including mortality, stunting, and growth failure. Recent evidence has demonstrated that the incidence of wasting and linear growth failure is highest between birth and 3 months of age, substantially earlier than previously thought. Interventions are urgently needed to improve outcomes in low birthweight babies; however, these interventions must not interfere with breastfeeding and thus some well-established interventions used to treat or prevent malnutrition in older children cannot be considered. The investigators recently demonstrated that biannual mass azithromycin distribution reduces all-cause childhood mortality by approximately 25% in infants aged 1-5 months, with stronger effects seen in underweight infants. This study did not include neonates due to the risk of infantile hypertrophic pyloric stenosis (IHPS) that has been hypothesized to be associated with macrolide use during early infancy. However, our study team documented only a single case of IHPS among 21,833 neonates enrolled in a trial of azithromycin versus placebo administered to neonates aged 8-27 days for prevention of infant mortality, documenting no major risk of IHPS associated with azithromycin. Here, the investigators propose an individually randomized trial where participants will receive a single oral dose of azithromycin (administered either during the neontal period or 21 days after enrollment), two does of oral azithromycin spaced 21 days apart, or two doses of placebo to evalute if azithromycin improves nutritional outcome and reduces infectious burden among neonates aged 1-27 days who are either low birthweight (\<2500 g at birth) or underweight (weight-for-age Z-score \< -2 at enrollment). The primary outcome will be weight-for-age Z-score at 6 months of age compared between arms. The investigators anticipate that the results of this study will provide definitive evidence on azithromycin as an early intervention for low birthweight/underweight neonates, who are at the highest risk of adverse outcomes.

2024-07-31

2027-07-31

2027-07-31

Not yet recruiting

Early phase I

5000

Inclusion Criteria: * Aged 1-27 days old * Birthweight \< 2500 g and/or weight-for-height Z score \<- 2 standard deviations at enrollment * Weigh at least \<1500 g at time of enrollment * Able to feed orally * Family intends to stay in the study area for at least 6 months * Appropriate consent from at least one caregiver * No known allergy to macrolides * No hepatic failure manifested by neonatal jaundice * Not currently an inpatient at the clinic * Not being transferred to a hospital for clinical complications Exclusion Criteria: * Birthweight \> 2500 g * Weigh less than 1500 g at time of enrollment * Unable to feed orally * Family planning to move within 6 months * Mother/ caregiver not willing to participate * Allergic to macrolides * Hepatic failure manifested by neonatal jaundice * Currently being seen as an inpatient at the clinic * Currently being transferred to a hospital for clinical complications

{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE4'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'FACTORIAL', 'primaryPurpose': 'PREVENTION', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 5000, 'type': 'ESTIMATED'}}

2023-12-04