Accelerometry at the Neck: Comparison With m. Adductor Pollicis Stimulation

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-04-30

Study Completion Date

2015-12-31

Brief Summary

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Accelerometric Assessment of neuromuscular block during anaesthesia is routinely performed at the M. adductor pollicis. However, many operations require positioning of the patients with arms attached to the body. In these situations, the anaesthesiologist has no access to the m.adductor pollicis.

In this study, a new position of accelerometry at the neck is evaluated: Stimulation of the n. accessorius with accelerometry of the m. trapezius.

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Detailed Description

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Conditions

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Feasibility of Measurement of a Neuromuscular Block at the m. Trapezius

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Blinding Strategy

NONE

Study Groups

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Group trapezius

Assessment of intubation conditions after onset of the neuromuscular block at the m. trapezius

Group Type OTHER

accelerometry m. trapezius and m. adductor pollicis

Intervention Type DEVICE

group adductor pollicis

assessment of intubation conditions after onset of the neuromuscular block at the m. adductor pollicis

Group Type OTHER

accelerometry m. trapezius and m. adductor pollicis

Intervention Type DEVICE

Interventions

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accelerometry m. trapezius and m. adductor pollicis

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Patients undergoing general anaesthesia with endotracheal intubation
* weight 50-90 kg

Exclusion Criteria

* Pregnancy
* allergy to one of the drugs used
* risk of pulmonary aspiration
* expected difficulties with endotracheal intubation
* intake of drugs known to influence neuromuscular block
* infection (CRP \> 0,5 mg/dl, leukocyte count \> 12000/µl)

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No