Last reviewed · How we verify

NCT04159116

Prevention and Treatment of Laryngospasm and Hypoxemia Based on Risk Factors in Adult Outpatients Undergoing EGD

Completed NA Last updated 17 March 2021
What this trial tests

NA trial testing Prophylactic suctioning when clinically indicated in Laryngospasm in 57 participants. Completed in 19 March 2020.

Timeline
4 November 2019
Primary endpoint
19 March 2020
19 March 2020

Quick facts

Lead sponsorEnvision Healthcare Scientific Intelligence, Inc.
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment57
Start date4 November 2019
Primary completion19 March 2020
Estimated completion19 March 2020
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Envision Healthcare Scientific Intelligence, Inc.

Who can join

18 and older, any sex, with Laryngospasm or Hypoxemia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to identify patient and provider-chosen factors that put patients at risk for the development of hypoxemia (oxygen saturation \< 90% for 5 seconds) during endoscopy and to use this knowledge to develop a treatment protocol for specific causes of hypoxemia in adult esophagogastroduodenoscopy outpatients.

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 Envision Healthcare Scientific Intelligence, Inc. 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/NCT04159116.

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