MedTrace Logo

Sedasys Post Approval Study Users Response to System Alarms

NCT02573818 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 51

Last updated 2017-03-24

No results posted yet for this study

Summary

The purpose of this study is to evaluate the users' responses to the SEDASYS® System alarms during esophagogastroduodenoscopy (EGD) or colonoscopy.

Conditions

  • Conscious Sedation

Interventions

DEVICE

SEDASYS System

propofol sedation with the SEDASYS System

Sponsors & Collaborators

  • Ethicon Endo-Surgery

    lead INDUSTRY

Principal Investigators

  • James F Martin, PhD · Ethicon Endo-Surgery, Inc.

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-09-01
Primary Completion
2016-06-15
Completion
2016-06-15
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

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 NCT02573818 on ClinicalTrials.gov