Peripheral Nerve Stimulation to Reduce Hypoxic Events
Completed · Not applicable · Has a placebo group
Conditions studied: Apnea, Hypoventilation, Hypoxemia
In brief
This study is designed to determine if using peripheral nerve stimulation in conjunction with pulse oximetry as an adjunct to traditional monitoring in the PACU reduces the frequency and severity of sedation related apnea and hypoxic events.
Key facts
- Study ID
- NCT02554110
- Run by
- Mayo Clinic
- People needed
- 80
- Starts
- 2015-10-12
- Expected to finish
- 2017-01-19
- Last updated by the study team
- 2018-11-15
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Males and females > 18 yrs old
- Flemon's Score > 15
- Able to provide written informed consent
- Having gynecological, colorectal, orthopedic surgery, and urologic surgeries
- Baseline oxygen saturation on room air > 96%
You may not qualify if…
- Peripheral neuropathy involving the upper extremities
- Procedures requiring direct admission to the ICU or any site other than the post-anesthesia care unit from the OR
- Diagnosed obstructive sleep apnea (OSA) and / or use of continuous positive airway pressure (CPAP) or biphasic positive airway pressure (BiPAP) in the PACU.
- Presence of any implantable electric devices, including internal defibrillators, pacemakers, or left ventricular assist device (LVAD)
- Post-procedure temperature < 35.5 Celsius or evidence of vasoconstriction
- Presence of metal hardware in either arm or in either shoulder
- Patients lacking access to the bare skin on an arm after surgery.
- History of atrial fibrillation
- History of bundle branch block
- Females from menarche to menopause that do not have a current negative pregnancy test or surgical history preventing pregnancy.
Where it is running
- Mayo Clinic in Rochester — Rochester, Minnesota, United States
Full record on ClinicalTrials.gov
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