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The TOF3D Mechanomyograph. Evaluation of a New Device for Assessment of the Neuromuscular Block.

The TOF3D Mechanomyograph. Evaluation of a New Device for Assessment of the Neuromuscular Block.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07371377
Acronym
MMG versus AMG
Enrollment
50
Registered
2026-01-27
Start date
2026-01-09
Completion date
2027-07-01
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mechanomyography, Neuromuscular Blockade Monitoring

Keywords

mechanomyography, tetanic fade

Brief summary

In clinical anesthesiologic practice, most institutions use acceleromyography in order to assess the degree of a neuromuscular block. The aim of the present study is to assess a new device using mechanomyography. Until recently, this method was reserved for experimental settings. It seems to be able to work more precisely, and additionally, it offers the opportunity to use other stimulation patterns than acceleromyographic measurements. The investigation is divided into two parts: Part 1 compares the mechanomyograph directly with an acceleromyograph. In part 2, two mechanomyographs using different stimulation patterns are compared with each other.

Interventions

DEVICEmeasurement of the time course of a neuromuscular block

a new device is compared to an established one.

Sponsors

Klinikum Hersfeld-Rotenburg
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* patients scheduled for surgery requiring general anesthesia with neuromuscular blocking agents

Exclusion criteria

* anticipated or known difficult airway * increased risk for aspiration * pregnancy * neuromuscular disorders

Design outcomes

Primary

MeasureTime frameDescription
difference in time to recovery to a train of four ratio of 1,0.from enrollment to the end of anesthesiologic treatment at the day of surgery (2-3 weeks after enrollment)difference in time to recovery to a train of four ratio of 1,0 measured by acceleromyography and mechanomyography, respectively

Countries

Germany

Contacts

CONTACTStefan Soltesz, Professor
stefan.soltesz@klinikum-hef.de0049 6621 88 922775

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026