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NCT04017702

Detection of Postoperative Respiratory Depression in High Risk Patients Utilizing Minute Ventilation Monitoring

Completed Last updated 1 April 2022
What this trial tests

trial testing Expiron respirator in Respiratory Depression in 86 participants. Completed in 20 February 2020.

Timeline
20 June 2018
Primary endpoint
20 February 2020
20 February 2020

Quick facts

Lead sponsorYale University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment86
Start date20 June 2018
Primary completion20 February 2020
Estimated completion20 February 2020
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Yale University

Who can join

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

Sponsor's own description

Respiratory volume monitor (RVM) (ExSpiron) is superior to continuous pulse oximetry in detection of postoperative respiratory depression in high risk patients.

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 recruiting trials for Respiratory Depression

Currently open trials in the same condition.

Other Yale University 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/NCT04017702.

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