Last reviewed · How we verify

NCT03819023

Validation of RespiLife for Detection of Respiratory Suppression

Completed NA Last updated 4 April 2019
What this trial tests

NA trial testing Respilife monitor in Respiration Disorders in 30 participants. Completed in 20 March 2019.

Timeline
20 December 2018
Primary endpoint
2 March 2019
20 March 2019

Quick facts

Lead sponsorBioresp Technologies, Inc.
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposediagnostic
Enrollment30
Start date20 December 2018
Primary completion2 March 2019
Estimated completion20 March 2019
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Bioresp Technologies, Inc.

Who can join

Adults 18 to 80, any sex, with Respiration Disorders. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to evaluate the accuracy of RespiLife diagnostic technology for detection of respiratory rate and oxygen saturation in human subjects. This includes evaluation of Bioresp's RespiLife and its accuracy for measurement of respiratory rate and oxygen saturation.

Publications & conference data

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

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Other recruiting trials for Respiration Disorders

Currently open trials in the same condition.

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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/NCT03819023.

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