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NCT03369197 · ClinicalTrials.gov registry record · NA

Nasal Continuous Positive Airway Pressure Versus Standard Care During Procedural Sedation for Gastrointestinal Endoscopy

A NA study, sponsored by Johns Hopkins University.

Completed
Registry status
NA
Development phase
111
Enrollment target

NCT03369197: Completed NA study, sponsored by Johns Hopkins University.

NCT03369197 is a NA study that has completed, run by Johns Hopkins University. The registered enrollment target is 111 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03369197, a NA study, has completed, sponsored by Johns Hopkins University.

COMPLETED
Registry status
NA
Development phase
111 participants
Enrollment target

Study Summary

This study is a randomized controlled trial comparing oxygen delivery by nasal mask with continuous positive airway pressure versus standard care (nasal cannula or standard facemask) during propofol-based sedation for gastrointestinal endoscopy procedures to reduce the incidence of hypoxia. The primary outcome will be the rate of oxygen desaturation below 90% for ≥15 seconds.

Interventions

  • DEVICE Nasal Mask
  • DEVICE Control: Nasal Cannula

Trial Details

FieldValue
Enrollment Target 111 participants
Start Date 2017-10-30
Est. Completion 2019-10-23
Phase NA

Sponsor

Johns Hopkins University

1,448 total trials

What the Registry Record Tells You About NCT03369197

The ClinicalTrials.gov registry entry for NCT03369197 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 111 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Johns Hopkins University, which has 1,448 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Nasal Mask is the first listed.

NCT03369197 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03369197 about?

NCT03369197 is a clinical study titled "Nasal Continuous Positive Airway Pressure Versus Standard Care During Procedural Sedation for Gastrointestinal Endoscopy". This study is a randomized controlled trial comparing oxygen delivery by nasal mask with continuous positive airway pressure versus standard care (nasal cannula or standard facemask) during propofol-based sedation for gastrointestinal endoscopy procedures to reduce the incidence of hypoxia. The prim...

What is the current status of trial NCT03369197?

This trial is currently completed. It is a NA study. The enrollment target is 111 participants. The study started on 2017-10-30. Estimated completion is 2019-10-23.

What interventions are being tested in trial NCT03369197?

The interventions under investigation include: Nasal Mask (DEVICE), Control: Nasal Cannula (DEVICE).

Who is sponsoring clinical trial NCT03369197?

This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.