Clinical Trials Logo

Clinical Trial Summary

This study investigates the incidence of postoperative respiratory complications (PRCs) including: oxygen desaturation events, tracheal re-intubations within 48 hours of surgery, and failure to wean from ventilator within 48 hours of surgery - in patients with and without risk factors for OSA undergoing elective, non-cardiac surgery (NCS).


Clinical Trial Description

324 subjects will be enrolled into one of two groups: increased or not increased risk for OSA, n=162 patients per group. Preoperative assessments of OSA status, Mallampati score (an assessment for mouth and throat morphology), STOP-BANG test (assessment for risk of OSA), and medical history will be used to determine patient group assignment. All subjects will receive standard general anesthesia and monitoring as a part of standard of care whether or not she/he will participate in the study, including ECG, arterial pressure, SpO2, BIS, Blood pressure (BP), heart rate (HR), and respiratory rate (RR), all of which will be continuously recorded and data will be saved for every three minutes during induction using standard monitors. Standard monitoring assessments in PACU will be used, and patients with increased perioperative risk for OSA will be closely monitored for hypoxemia and other complications. The Nellcor Pulse Oximetry Sensor will be applied in PACU and continuously monitor the patient's oxygen saturation and respiratory rate for the first 48 hours postoperatively. At the end of the 48 hours, the device will be removed, and the de-identified data will be transferred to a computer with analysis software and examined for patterns in respiratory distress in both patient groups. Data collected from the Nellcor Bedside Respiratory Patient Monitoring System on pulse and oxygen saturation, as well as data on clinically significant events, such as PRCs, acute respiratory failure, tracheal reintubation, hypoxemia, CHF, MI, A-fib, and delirium will be analyzed to understand the effects of OSA on postoperative recovery ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02729077
Study type Observational
Source Ohio State University
Contact
Status Completed
Phase
Start date July 2016
Completion date February 4, 2021

See also
  Status Clinical Trial Phase
Recruiting NCT04596735 - Extubation Criteria in Patients Greater Than 59 Years of Age
Withdrawn NCT02460055 - Trial- Dysphagia From ETT or GI Endoscopy N/A
Completed NCT02336022 - The Evaluation of a Noninvasive Respiratory Monitor in Pediatric Patients Undergoing General Anesthesia N/A
Completed NCT02256384 - Evaluation of Respiratory Acoustic Monitor in Children After Surgery N/A
Completed NCT02060994 - Respiratory Morbidity Among Children Who Were Born by Elective Cesarean Section After 37-38 Weeks vs. 39 Weeks and More N/A
Completed NCT02899351 - The Evaluation of a Noninvasive Respiratory Monitor in Intubated Infants