Trials / Terminated
TerminatedNCT02573818
Sedasys Post Approval Study Users Response to System Alarms
Open-Label Post Approval Study of the SEDASYS System User Response to System Alarms
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 51 (actual)
- Sponsor
- Ethicon Endo-Surgery · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to evaluate the users' responses to the SEDASYS® System alarms during esophagogastroduodenoscopy (EGD) or colonoscopy.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | SEDASYS System | propofol sedation with the SEDASYS System |
Timeline
- Start date
- 2015-09-01
- Primary completion
- 2016-06-15
- Completion
- 2016-06-15
- First posted
- 2015-10-12
- Last updated
- 2017-03-24
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT02573818. Inclusion in this directory is not an endorsement.