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The purpose of this study is to compare two neuromuscular blockade monitors on recovery from an ATRACURIUM intra veinous injection for surgery. The TOFscan, a wired connected monitors and the WiTOF, a wireless connected monitor.
The secondary objective will be to compare the performance of the two monitors on the abductor pollicis muscle with all the curarisation parameters (TOF, PTC, T4/T1R) and to assess interference occuring during the surgery which could limit the usage of a wireless monitor.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| WiTOF | Experimental |
| |
| TOFscan | Active Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| WiTOF | Device | Data collection on the WiTOF monitor |
| |
| TOFscan |
| Measure | Description | Time Frame |
|---|---|---|
| Evaluate the neuromuscular blockade recovery after intraveinous injection of atracurium with 2 differents monitors. | Comparison on the obtention delay for the T4/T1 ratio superior ou equal to 90% beetween the WiTOF and the TOFScan | During the whole period of the surgical operation maximum 8 hours |
| Measure | Description | Time Frame |
|---|---|---|
| Evaluate the performance of the monitors for the follow up of neuromuscular recovery | Comparison of neuromuscular blockade parameters obtained with the WiTOF and the TOFScan (TOF, PTC, T4/1R) | During the whole period of the surgical operation maximum 8 hours |
| Number and duration of perturbation from the surgical environnement that could limit the usage of a wireless monitor |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Matthieu BOISSON | CHU de Poitiers FRANCE | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CHU de Poitiers | Poitiers | 86021 | France |
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| Device |
Data collection on the TOFscan monitor |
|
Assess what could perturbate the data collection on the wireless monitor |
| During the whole period of the surgical operation maximum 8 hours |