Trials / Completed
CompletedNCT03847740
Safety and Feasibility of a New Neuromuscular Monitoring Device
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 15 (actual)
- Sponsor
- Poitiers University Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 100 Years
- Healthy volunteers
- Not accepted
Summary
The aim of the study is to compare, during general anesthesia using neuromuscular blocking agent, the feasibility of a new mechanographic device (ITF handle and Visual ITF software) with a standard acceleromyographic device (TOF Watch SX) and also to assess its safety during the first 24 hours after surgery. The two devices will be studied simultaneously in each patient.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Isometric Trumb Force handle | Compare the pattern of neuromuscular blocking drug between two devices applied on the same patient during general anesthesia. |
Timeline
- Start date
- 2019-02-22
- Primary completion
- 2019-08-22
- Completion
- 2019-08-22
- First posted
- 2019-02-20
- Last updated
- 2019-10-31
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT03847740. Inclusion in this directory is not an endorsement.