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NCT07283354Not yet recruiting

Comparison of Acceleromyography and Electromyography in Obese Patients Undergoing General Anesthesia

Comparison of Acceleromyography and Electromyography in Obese Patients Undergoing General Anesthesia With Rocuronium: A Prospective Observational Study

Source: ClinicalTrials.gov · Last updated 15 Dec 2025

Brief summary (registry, in English)

The goal of this prospective observational study is to compare two different methods of monitoring muscle relaxation during anesthesia - acceleromyography (AMG) and electromyography (EMG) - in people with obesity who are having bariatric surgery with general anesthesia and the muscle relaxant rocuronium. The main question is: Which method is more accurate and precise in measuring the Train-of-Four (TOF) ratio during surgery? As part of this comparison, researchers will also note how quickly each method detects recovery of muscle function after the reversal drug sugammadex. Participants will: * Receive standard anesthesia care for bariatric surgery, including rocuronium to relax the muscles. * Have two small monitoring devices applied, one to each hand: AMG on one hand, EMG on the other. * Be monitored for muscle function during surgery and after receiving sugammadex to reverse the muscle relaxation. Researchers will also record how easy each device is to use and whether participants have any breathing problems after surgery.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
30 (estimated)
First submitted
25 Nov 2025
Start date
1 Feb 2026
Primary completion date
30 Jul 2026
Lead sponsor
University of Padova
Diseases
Obesity
NCT number
NCT07283354

What you commit to

  • Study type: Observational
  • Planned participants: 30
  • From 1 Feb 2026 to the primary completion date, 30 Jul 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Severe acute or chronic respiratory disease (e.g., asthma, COPD, severe restrictive disease)
  • Severe acute or recent cardiac disease (e.g., acute or recent myocardial infarction, inducible ischemia, heart failure)
  • End-stage hepatic or renal disease
  • Intolerance, allergy, or contraindication to study-related drugs

Other

  • Absence of informed consent

Who the study is looking for

  • Adults aged 18-65 years
  • Pathological obesity (Class II with comorbidities or Class III)
  • Scheduled for bariatric surgery under general anesthesia
  • Written informed consent obtained

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Azienda Ospedale - Università di Padova (Padua University Hospital)
Coordinator of this site? Confirm its status
PadovaItalyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.