Comparison of the TOFScan and the WiTOF During Recovery of Neuromuscular Function

Poitiers University Hospital

Status: Completed

Conditions: Neuromuscular Residual Curarization

Treatments: Device: TOFscan; Device: WiTOF

Study type: Interventional

Funder types: Other

Identifiers

NCT05231525

WiTOF

Details and patient eligibility

About

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.

Full description

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.

Enrollment: 80 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• All programmed surgery with intraveinous injection of ATRACURIUM
• American society of anesthesiology patient score of I, II or III
• Patient being free of tutorship or curatorship
• Acceptance of the patient after clear and loyal information

Exclusion criteria

• Surgery without access simultaneously to the two arms
• Emergency surgery
• Rapid sequence induction
• Usage of an other curare than ATRACURIUM
• Contraindication on ATRACURIUM usage
• Patient with pace maker
• Patient with Arné score > or = to 11
• Patient without social security coverage
• Pregnant of breastfeeding women
• Patient under social protection

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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80 participants in 2 patient groups

WiTOF

Experimental group

Treatment:

Device: WiTOF

TOFscan

Active Comparator group

Treatment:

Device: TOFscan