A Randomized, Double-Blind, Comparative Trial of Stimulation Electrode Placement during Electromyography-based Neuromuscular Monitoring (Pilot Study)
Not Applicable
- Conditions
- Patients with upper gastrointestinal, lower gastrointestinal, hepatobiliary, gynecologic, or urologic diseases undergoing laparoscopic surgery in the 0 degrees pronation in both upper limb position
- Registration Number
- JPRN-UMIN000051981
- Lead Sponsor
- agasaki University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 32
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who already have neurological disorders (e.g., paralysis) Patients with neuromuscular diseases Patients with pacemakers or implantable cardioverter defibrillators Pregnant women Patients with fragile skin where the electromyography electrode seal is applied Patients with a history of surgery on the measuring limb Patients with a history of allergy to Rocuronium or Sugammadex Patients undergoing hemodialysis Patients undergoing robot-assisted laparoscopic surgery
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method