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EMG ss AMG In Robotic/Laparoscopic Surgery

NCT07525323 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 400

Last updated 2026-05-06

No results posted yet for this study

Summary

The purpose of this study is to compare the mean cumulative weight-based/time-corrected rocuronium dose administered in patients undergoing robotic- or laparoscopic- assisted surgery using either acceleromyography or electromyography.

Conditions

  • Surgery

Interventions

DEVICE

AMG device

The anesthesia team will use an AMG device to monitor neuromuscular block

DEVICE

EMG

The anesthesia team will use an EMG device to monitor neuromuscular block

Sponsors & Collaborators

Principal Investigators

  • Johnathan Renew · Mayo Clinic

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-05-31
Primary Completion
2026-12-31
Completion
2026-12-31
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07525323 on ClinicalTrials.gov