The Effect of Wearable Neuromuscular Electrical Stimulation in Major Abdominal Surgery: A Randomized Clinical Trial
Not Applicable
Recruiting
- Conditions
- Gastrointestinal cancer
- Registration Number
- JPRN-UMIN000041307
- Lead Sponsor
- Aichi Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Not provided
Exclusion Criteria
(1) Eastern Cooperative Oncology (ECOG) performance status (PS) 3 or higher (2) Patients with neuromuscular disease (3) Patients using electrical medical equipment such as pacemakers (4) Patients who cannot use the skeletal muscle electrical stimulator due to metal inclusions (5) Patients expected to require management in the intensive care unit for 2 days or more after surgery (6) Patients who are pregnant or may be pregnant (7) In addition, patients judged to be unsuitable for this study by the principal investigator or the doctor
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Rate of change in quadriceps area
- Secondary Outcome Measures
Name Time Method