drugset / Trial / NCT00189007

Antenatal Allopurinol During Fetal Hypoxia

NCT00189007 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

A former study (submitted) in 32 severely asphyxiated infants participating in a randomized double blind study, in which early postnatal allopurinol or a placebo (within 4 hours after birth) was administered to reduce free radical formation and consequently reperfusion/reoxygenation injury to the newborn brain, showed an unaltered high mortality and no clinically relevant improvement in morbidity in infants treated with allopurinol. It was hypothesized that postnatal allopurinol treatment started too late to reduce reperfusion-induced free radical surge and that initiating allopurinol treatment of the fetus with (imminent) hypoxia already via the mother during labor will be more effective to reduce free radical-induced post-asphyxial brain damage.

Timeline

Start
2009-10
Primary completion
2011-12
Completion
2016-12

Outcome

Missed primary endpoint

paper Cord S100ß was not significantly different between the two groups: 44.5 pg/mL (IQR 20.2-71.4) in the ALLO group versus 54.9 pg/mL PMID 25512466 ↗

paper Maternal treatment with allopurinol during fetal hypoxia did not significantly lower neuronal damage markers in cord blood. PMID 25512466 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Allopurinol Small molecule 500 mg Intravenous