Remote Oximeter Monitoring Post-discharge to Reduce Emergency Room Visits and Rehospitalization

Study acronym: ROMPER
StatusEnrolling by Invitation
PhaseNot applicable
Started

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Record History

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  1. Trial status changed: Recruiting → Enrolling by Invitation
    • Eligibility criteria expanded, about 6 words
    • Secondary endpoints: details revised at 1 of 11 entries
    • Site details revised
  2. Start date changed from estimate of Sep 9, 2025 to Sep 11, 2025v8
  3. Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    • Start date: Aug 17, 2025 to Sep 9, 2025
    v7
  4. Start date: Aug 1, 2025 to Aug 17, 2025v6
  5. Start date: Jul 1, 2025 to Aug 1, 2025v5
Show 3 earlier versionsHide 3 earlier versions
  1. Start date: Mar 1, 2025 to Jul 1, 2025v4
  2. Start date: Jan 1, 2025 to Mar 1, 2025v3
  3. Start date: Oct 1, 2024 to Jan 1, 2025v2
  1. Study First Submitted
  • 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.
This randomized clinical trial will determine the efficacy of remote patient monitoring using an Owlet OSS 3.0 pulse oximeter for the reduction of emergency room visits and high-acuity rehospitalizations among high-risk infants after NICU discharge.
Trial Details
NCT Number NCT06565390
Lead Sponsor University of Alabama at Birmingham
Collaborators: Owlet Baby Care, Inc.
Conditions
(from sponsor)		 Emergencies
Related terms Emergencies
Enrollment 700 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov