EMG ss AMG In Robotic/Laparoscopic Surgery

Part of paid clinical trials in Jacksonville, Florida.

Sponsor
Mayo Clinic
Study ID
NCT07525323
Status
Enrolling By Invitation

Conditions

  • Surgery

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • AMG device — DEVICE
    The anesthesia team will use an AMG device to monitor neuromuscular block
  • EMG — DEVICE
    The anesthesia team will use an EMG device to monitor neuromuscular block

Study Details

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.

Key Dates

Start date
May 31, 2026
Status verified
May 2026
Primary completion
Dec 31, 2026
Completion
Dec 31, 2026

Study Design

Enrollment
400 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER

Arms

  • Experimental: AMG
    The anesthesia team will manage the level of block based on AMG values
  • Active Comparator: EMG
    The anesthesia team will manage the level of block based on EMG values

Primary Outcome Measure

Cumulative rocuronium dose [ Time Frame: Perioperative/Periprocedural ]

Locations (1)

FacilityCityStateZIPSite coordinators
Mayo Clinic in FloridaJacksonvilleFlorida32224-

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