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NCT03774199: NPOCS

NightOwl Pulse Oximeter Calibration Study

Status unknown NA Last updated 21 March 2019
What this trial tests

NA trial testing NightOwl in Pulse Oximeter Calibration in 30 participants. Status unknown.

Timeline
14 December 2018
Primary endpoint
14 December 2019
14 April 2020

Quick facts

Lead sponsorEctosense NV
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposebasic science
Enrollment30
Start date14 December 2018
Primary completion14 December 2019
Estimated completion14 April 2020
Sites1 location across Belgium

Drugs / interventions tested

Conditions studied

Sponsor

Ectosense NV

Who can join

13 and older, any sex, with Pulse Oximeter Calibration. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Calibration of a software module that computes SpO2 based on photoplethysmography (PPG) traces acquired by a reflectance-based pulse oximeter which can be placed on the index finger or the forehead. The study is designed in accordance with Medical electrical equipment - Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment (ISO 80601- 2-61:2011)

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of NightOwl

Trials testing the same drug.

Other Ectosense NV 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/NCT03774199.

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