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Nausea and Vomiting in Postoperative Paediatric Patients With Patient-Controlled Analgesia (PCA): Morphine vs Oxycodone

Study acronym: POPCORN
StatusRecruiting
PhasePhase 4
Started
View on ClinicalTrials.gov ↗

Record History

  1. Re-verified, no change to tracked fieldsv6
  2. Primary completion date: Mar 19, 2026 to Dec 2027 Completion date: Mar 19, 2027 to Dec 2027v5 Show 1 more changeShow less
    • Completion date: Mar 19, 2027 to Dec 2027
  3. Re-verified, no change to tracked fieldsv4
  4. Trial status: Not Yet Recruiting to Recruiting Primary completion date: Mar 2026 to Mar 19, 2026 · Completion date: Mar 2027 to Mar 19, 2027 · Start date changed from estimate of Mar 2024 to Mar 13, 2024 · 1 morev3 Show 4 more changesShow less
    • Primary completion date: Mar 2026 to Mar 19, 2026
    • Completion date: Mar 2027 to Mar 19, 2027
    • Start date changed from estimate of Mar 2024 to Mar 13, 2024
    • Site details revised
  5. Start date: Jan 2024 to Mar 2024 Primary completion date: Jan 2026 to Mar 2026v2 Show 1 more changeShow less
    • Primary completion date: Jan 2026 to Mar 2026
  6. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
POPCORN trial will compare the side effects and effectiveness of Morphine versus Oxycodone medication when prescribed for use as patient controlled analgesia (PCA) for pain relief for paediatric patients after-surgery. This trial is embedded into routine patient care using the hospital electronic medical record (EMR). Participants will be randomly assigned to either medication after they enrol in the study. The main questions the POPCORN trial aims to answer are: * 1\. Is there a difference in the usage of medication to treat nausea and vomiting for those who received oxycodone PCA versus morphine PCA for post-surgery pain relief? * 2\. Is there a difference in side effects or pain relief needed between the two groups? Study activities are as follows: * Participants enrolled to study during their pre-operative consultation * Participants are randomly assigned to morphine or oxycodone * No further study-specific activities expected from participant after enrolment and randomisation * Participant receives routine medical care as planned * Clinicians record assessments as per routine care in electronic medical record (EMR) * EMR data are extracted as trial data
Trial Details
NCT Number NCT06186141
Lead Sponsor Murdoch Childrens Research Institute
Conditions Patient-Controlled Analgesia
Enrollment 690 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov