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Safety and Efficacy of the LMA Supreme When Inserted With Patients in the Prone Position

NCT03633942 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2018-08-24

No results posted yet for this study

Summary

This study is a non-randomized, observational, non-comparative prospective study to evaluate the safety, efficacy and performance of the LMA Supreme laryngeal mask airway when used according to the device's Instructions for Use.

Conditions

  • Airway Obstruction

Interventions

DEVICE

LMA Supreme

Placement of the LMA Supreme supraglottic airway device for patients undergoing outpatient spine surgery in the prone position.

Sponsors & Collaborators

  • Teleflex

    collaborator INDUSTRY

  • Laser Spine Institute

    lead INDUSTRY

Principal Investigators

  • Thor Van Diver, MD · Laser Spine Institute

  • George Lin, MD · Laser Spine Institute

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-07-27
Primary Completion
2019-07-27
Completion
2020-07-27
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03633942 on ClinicalTrials.gov