No side-effects of single intranasal oxytocin administration in middle childhood

Martine W.F.T. Verhees*, Janne Houben, Eva Ceulemans, Marian J. Bakermans-Kranenburg, Marinus H. van IJzendoorn, Guy Bosmans

*Corresponding author for this work

Research output: Contribution to JournalArticleAcademicpeer-review

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Abstract

Background: Despite growing interest in the (therapeutic) use of intranasal oxytocin administration in children, the potential side-effects of intranasal oxytocin have remained largely unclear to date. The current study is the first double-blind randomized controlled trial to examine side-effects following single administration of oxytocin nasal spray in elementary school-aged children. Methods: One hundred children (8–12 years old) were randomly assigned to receive oxytocin or placebo nasal spray. We assessed side-effects by means of a standardized, drug-specific questionnaire and an open-ended question at two time points: 90 min after nasal spray administration and 24 h after administration. Results: There were no significant associations between nasal spray condition and total frequency of reported side-effects or reports of specific side-effects. Children and their mothers were unable to correctly guess nasal spray allocation, further supporting that the subjective experience of oxytocin versus placebo nasal spray effects was similar. Moreover, the majority of reported side-effects were classified as mild and ceased within 24 h after the procedure, indicating that the nasal sprays were well tolerated. Conclusion: In all, this study is the first randomized controlled trial to provide information on the safety of intranasal oxytocin administration in middle childhood. The current study suggests that single administration of intranasal oxytocin is likely safe in elementary school-aged children.

Original languageEnglish
Pages (from-to)2471-2477
Number of pages7
JournalPsychopharmacology
Volume235
Issue number8
DOIs
Publication statusPublished - 1 Aug 2018

Funding

Funding information This work was supported by grants G.0774.15 and G.0757.18 from Research Foundation Flanders (FWO) and CREA/12/ 004 from Research Fund KU Leuven. MJBK was supported by an Advanced Grant from the European Research Council.

FundersFunder number
Horizon 2020 Framework Programme669249
European Research Council
Fonds Wetenschappelijk OnderzoekG.0774.15, G.0757.18
KU LeuvenCREA/12/ 004

    Keywords

    • Intranasal administration
    • Middle childhood
    • Oxytocin
    • Randomized controlled trial
    • Side-effects

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