Electromyographic Assessment of the TetraGraph in Normal Volunteers

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Mayo Clinic

Status

Completed

Conditions

Neuromuscular Blockade

Treatments

Device: TetraGraph
Device: TOF Watch

Study type

Observational

Funder types

Other

Identifiers

NCT02912039
16-005022

Details and patient eligibility

About

There is an urgent need for an easy-to-use and accurate quantitative neuromuscular monitor in the clinical setting. The aim of this clinical investigation is to examine a prototype of a quantitative monitoring instrument that will meet most, if not all, of the clinical requirements.

Enrollment

45 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

  • Age 18 years or older
  • Volunteer meets the American Society of Anesthesiology (ASA) physical status I-III criteria
  • Volunteer has provided verbal informed consent

Exclusion Criteria

  • Presence of an underlying neuromuscular disease
  • Use of medications known to interfere with neuromuscular transmission
  • Volunteer has open sores/rashes at the locations needed for electrode application
  • Volunteer does not tolerate a trial electrical stimulation comfortably.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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