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NCT03920670 · ClinicalTrials.gov registry record · NA

Comparison of the ToFscan and TetraGraph During Recovery of Neuromuscular Function in the Post Anesthesia Care Unit

A NA study, sponsored by Mayo Clinic.

Completed
Registry status
NA
Development phase
120
Enrollment target

NCT03920670: Completed NA study, sponsored by Mayo Clinic.

NCT03920670 is a NA study that has completed, run by Mayo Clinic. The registered enrollment target is 120 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT03920670, a NA study, has completed, sponsored by Mayo Clinic.

COMPLETED
Registry status
NA
Development phase
120 participants
Enrollment target

Study Summary

The aim of this investigation is to compare the performance of two quantitative monitors utilized on post-anesthesia recovering patients. The ToFscan (Draeger Medical Inc., Telford, PA) represents one of the few standalone acceleromyography (AMG)-based quantitative monitors available for routine clinical use in the United States. The TetraGraph (Senzime AB, Uppsala, Sweden) is a standalone electromyography (EMG)-based quantitative monitor that recently received Conformité Européene (CE) approval. While both of these quantitative monitors can be utilized to guide intraoperative NMBA re-dosing and confirm recovery, they provide their objective data via drastically different techniques.

Primary Outcome

Train-of-four ratios is the ratio of the fourth muscle response to the first one.

Interventions

  • DEVICE TetraGraph (TG)
  • DEVICE ToFscan (TS)

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2019-02-28
Est. Completion 2020-11-30
Phase NA
Mayo Clinic

2,844 total trials

What the finished NCT03920670 record still lists

NCT03920670 is an interventional study that assigns participants to a tested intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower).

The record links to 0 conditions, and to 2 interventions - of which TetraGraph (TG) is the first listed.

NCT03920670 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03920670 about?

NCT03920670 is a clinical study titled "Comparison of the ToFscan and TetraGraph During Recovery of Neuromuscular Function in the Post Anesthesia Care Unit". The aim of this investigation is to compare the performance of two quantitative monitors utilized on post-anesthesia recovering patients. The ToFscan (Draeger Medical Inc., Telford, PA) represents one of the few standalone acceleromyography (AMG)-based quantitative monitors available for routine cli...

What is the current status of trial NCT03920670?

This trial is currently completed. It is a NA study. The enrollment target is 120 participants. The study started on 2019-02-28. Estimated completion is 2020-11-30.

What interventions are being tested in trial NCT03920670?

The interventions under investigation include: TetraGraph (TG) (DEVICE), ToFscan (TS) (DEVICE).

Who is sponsoring clinical trial NCT03920670?

This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03920670's enrollment target sits among peer trials

120 762nd of 2000 higher than 1,198 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03920670, the US trial registry maintained by the National Library of Medicine. NCT03920670 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.