Last reviewed · How we verify

NCT06917326

Study to Assess Safety and Performance of Neola®, a Novel Lung Monitoring Device for Neonates

Completed NA Last updated 18 March 2026
What this trial tests

NA trial testing Monitoring in RDS of Prematurity in 10 participants. Completed in 12 March 2026.

Timeline
20 May 2025
Primary endpoint
12 March 2026
12 March 2026

Quick facts

Lead sponsorNeola Medical AB
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeother
Enrollment10
Start date20 May 2025
Primary completion12 March 2026
Estimated completion12 March 2026
Sites1 location across Sweden

Drugs / interventions tested

Conditions studied

Sponsor

Neola Medical AB — full company profile →

Who can join

Adults 1 Day to 14 Days, any sex, with RDS of Prematurity or Preterm Birth. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Clinical pilot study to assess safety and performance of Neola®, a novel lung monitoring device for neonates

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Monitoring

Trials testing the same drug.

Other recruiting trials for RDS of Prematurity

Currently open trials in the same condition.

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/NCT06917326.

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