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NCT06565390: ROMPER

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

Recruiting now NA Last updated 30 September 2025
What this trial tests

NA trial testing Babies in the Owlet monitor group in Emergencies in 700 participants. Currently enrolling.

Timeline
11 September 2025
Primary endpoint
31 October 2027
31 December 2030

Quick facts

Lead sponsorUniversity of Alabama at Birmingham
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposesupportive care
Enrollment700
Start date11 September 2025
Primary completion31 October 2027
Estimated completion31 December 2030
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of Alabama at Birmingham

Who can join

Adults 22 Weeks to 6 Months, any sex, with Emergencies. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Emergencies

Currently open trials in the same condition.

Other University of Alabama at Birmingham trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06565390.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing