Doxapram Therapy in Preterm Infants (DOXA Trial)

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age23-29
SponsorErasmus Medical Center

About this trial

Preterm infants often suffer from apnea of prematurity (AOP; a cessation of breathing) due to immaturity of the respiratory system. AOP can lead to oxygen shortage and a low heart rate which might harm the development of the newborn, especially the central nervous system. In order to prevent oxygen shortage, infants are treated with non-invasive respiratory support and caffeine. Despite these treatments, many preterm newborns still suffer from AOP and need invasive mechanical ventilation. Although this will result in complete resolution of AOP, invasive mechanical ventilation has the disadvantage of being a major risk of chronic lung disease and impaired neurodevelopmental outcome. Restrictive invasive ventilation is therefore advocated nowadays in preterm infants. Doxapram is a respiratory stimulant that has been administered off-label to treat AOP. Doxapram, as add-on treatment, seems to be effective in treating AOP and to prevent invasive mechanical ventilation. It is unclear if a preterm infant benefit from doxapram treatment on the longer term. This study compares doxapram to placebo and hypothesizes that doxapram will protect preterm infants from both invasive ventilation (and related lung disease) and AOP related oxygen shortage (and related impaired brain development).

Eligibility criteria

Qualifiers

Admitted to the neonatal intensvie care unit (NICU) of one of the participating centres

Written informed consent of both parents or legal representatives

Gestational age at birth < 29 weeks

Caffeine therapy, adequately dosed (see also under co-medication)

Disqualifiers

Previous use of open label doxapram

Use of theophylline (to replace doxapram)

Chromosomal defects (e.g. trisomy 13, 18, or 21)

Major congenital malformations that: compromise lung function (e.g. surfactant protein deficiencies, congenital diaphragmatic hernia); result in chronic ventilation (e.g. Pierre Robin sequence); increase the risk of death or adverse neurodevelopmental outcome (congenital cerebral malformations, chromosomal abnormalities);

Trial design

Treatments tested in this trial

  • Doxapram
  • Placebo

Treatment groups

396 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Erasmus Medical Center

Lead sponsor

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Collaborator

Nederlands Neonataal Netwerk (N3), the Netherlands

Collaborator

Universitaire Ziekenhuizen KU Leuven

Collaborator

Maternal, Infant, Child and Youth Research Network (MICYRN)

Collaborator