Track this trial free. DataLookout checks ClinicalTrials.gov daily and emails you which fields changed on NCT06824961 (status, enrollment, completion dates, endpoints, sites) when this record is updated. Free accounts track up to 5 trials.

Track this trial

Does Increasing the Compression Pause From 3 to 5 Seconds in Mechanical Compression Devices Increase Ventilation Success Rate and Return of Spontaneous Circulation?

Study acronym: LUCASVP
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 4 months later Sep 1, 2026 → Jan 15, 2027
See other at-risk trials from Amsterdam UMC, location VUmc

Record History

  1. Notable Recruitment openedv2 Show 4 more changesShow less
    • Start date changed from estimate of Mar 1, 2025 to Jan 15, 2026
    • Primary completion pushed from Sep 1, 2026 to Jan 15, 2027
    • Study completion pushed from Apr 1, 2027 to Jul 2027
    • Site details revised at 2 of 2 sites
  2. Minor 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
To give chest compressions during cardiopulmonary resuscitation (CPR), mechanical chest compression devices can be used. During synchronous 30:2 CPR, the standard setting on these devices leave an automated 3-second chest compression pause after 30 compressions to facilitate caregivers in providing two ventilations. With this standard setting, research has shown that in less than half of ventilation pauses during CPR, those two ventilations are given. Increasing the ventilation pause duration to 5 seconds instead of 3 seconds is also an option following current guideline recommendations, and aligns with measured ventilation pause duration in manual CPR. Increasing pause duration to 5 seconds could result in an increased ventilation success rate. This multicenter randomized controlled trial will randomize LUCAS® mechanical compression devices to a standard setting of 3- or 5-second compression pauses. The main outcome will be the percentage of ventilation pauses in which two ventilations are successfully given. Secondary outcomes include the restoration of spontaneous circulation (ROSC), and the difference in (neurologically intact) survival. No study has been performed to evaluate this effect yet.
Trial Details
NCT Number NCT06824961
Lead Sponsor Amsterdam UMC, location VUmc
Conditions
(from sponsor)
Cardiac Arrest (CA)
Related terms Heart Arrest, Out-of-Hospital Cardiac Arrest, Respiratory Aspiration
Enrollment 692 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov