Intravenous MELAtonin for prevention of Postoperative Agitation and Emergence Delirium in children (MELA‐PAED): A protocol and statistical analysis plan for a randomized clinical trial

Author:

Garioud Anne Louise de Barros12ORCID,Andersen Lars Peter Kloster23ORCID,Jensen Aksel Karl Georg4ORCID,Do Hien Quoc1ORCID,Jakobsen Janus Christian56ORCID,Holst Lars Broksø1ORCID,Rasmussen Lars Simon7ORCID,Afshari Arash12ORCID

Affiliation:

1. Department of Anesthesiology, Juliane Marie Center Copenhagen University Hospital—Rigshospitalet Copenhagen Denmark

2. Department of Clinical Medicine University of Copenhagen Copenhagen Denmark

3. Department of Anesthesiology Zealand University Hospital Køge Denmark

4. Section of Biostatistics, Department of Public Health University of Copenhagen Copenhagen Denmark

5. Copenhagen Trial Unit Centre for Clinical Intervention Research Copenhagen Denmark

6. Department of Regional Health Research, The Faculty of Health Sciences University of Southern Denmark Odense Denmark

7. Danish Ministry of Defence Personnel Agency Copenhagen Denmark

Abstract

AbstractBackgroundEmergence agitation and delirium in children remain a common clinical challenge in the post‐anesthetic care unit. Preoperative oral melatonin has been suggested as an effective preventive drug with a favorable safety profile. The oral bioavailability of melatonin, however, is low. Therefore, the MELA‐PAED trial aims to investigate the efficacy and safety of intraoperative intravenous melatonin for the prevention of emergence agitation in pediatric surgical patients.MethodsMELA‐PAED is a randomized, double‐blind, parallel two‐arm, multi‐center, superiority trial comparing intravenous melatonin with placebo. Four hundred participants aged 1–6 years will be randomized 1:1 to either the intervention or placebo. The intervention consists of intravenous melatonin 0.15 mg/kg administered approximately 30 min before the end of surgery. Participants will be monitored in the post‐anesthetic care unit (PACU), and the Post Hospitalization Behavior Questionnaire for Ambulatory Surgery (PHBQ‐AS) will be performed on days 1, 7, and 14 after the intervention. Serious Adverse Events (SAE) will be assessed up to 30 days after the intervention.ResultsThe primary outcome is the incidence of emergence agitation, assessed dichotomously as any Watcha score >2 during the participant's stay in the post‐anesthetic care unit. Secondary outcomes are opioid consumption in the post‐anesthetic care unit and adverse events. Exploratory outcomes include SAEs, postoperative pain, postoperative nausea and vomiting, and time to awakening, to first oral intake, and to discharge readiness.ConclusionThe MELA‐PAED trial investigates the efficacy of intravenous intraoperative melatonin for the prevention of emergence agitation in pediatric surgical patients. Results may provide further knowledge concerning the use of melatonin in pediatric perioperative care.

Funder

Dagmar Marshalls Fond

Kong Christian den Tiendes Fond

Rigshospitalet

Publisher

Wiley

Subject

Anesthesiology and Pain Medicine,General Medicine

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