EPAD Monitoring of Patients Undergoing Robotic Assisted Laparoscopic Genitourinary Surgery
- Conditions
- Surgery
- Interventions
- Device: EPAD monitoring system
- Registration Number
- NCT03319407
- Lead Sponsor
- Mayo Clinic
- Brief Summary
Participants to be enrolled in this study will have been scheduled to have laparoscopic genitourinary surgery and EPAD monitoring as part of their clinical care intraoperatively. Patients scheduled for genitourinary surgery are often at risk for developing nerve injuries due to intraoperative positioning.
Somatosensory evoked potential devices (SSEP) are commonly used to detect pending injury to peripheral nerves. The purpose of the present study is to use SSEP monitoring to determine the incidence and potential causes of significant changes in SSEP waveforms and correlate these changes with neurologic status of the brachial plexus after robotic surgery.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 21
- Patients scheduled to undergo robotic assisted laparoscopic genitourinary surgery
- Patients who are scheduled to have EPAD monitoring as part of their clinical care intraoperatively
• Patients with previous history of polyneuropathy, carpal tunnel, ulnar neuropathy, or similar neurological deficiencies
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Observation EPAD monitoring system All participants will be monitored with EPAD system
- Primary Outcome Measures
Name Time Method Somatosensory Evoked Potential Monitoring in the first 24 hours of postoperative period Recording of somatosensory evoked potential in patients undergoing genitourinary surgery
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Mayo Clinic Florida
🇺🇸Jacksonville, Florida, United States