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Peripheral Nerve Stimulation to Reduce Hypoxic Events

Hypoxemia Clinical Trial

Official title:
A Randomized Control Trial of the Oxistimulator as an Adjunct to Standard Practice to Decrease Extent and Duration of Oxygen Desaturation in Adult Patients Who Have Received Anesthetics or Are Receiving Sedating Medications

Clinical Trial Summary

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.

Clinical Trial Description

The primary effectiveness objective is to determine if transcutaneous stimulation will generate a respiratory response capable of reducing the extent and duration of oxygen desaturations in patients with presumed risk of obstructive sleep apnea (OSA) who have received some form of anesthesia or sedation. The primary safety objective is the demonstration that the peripheral nerve stimulation is safe for the use of preventing or reducing the sedation related hypoxemic events. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02554110
Study type Interventional
Source Mayo Clinic
Contact
Status Completed
Phase N/A
Start date October 12, 2015
Completion date January 19, 2017
View Details
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