auto-titrated CPAP
DevicePatients will be treated with auto-CPAP preoperatively for 2-3 nights preoperatively and 5 nights postoperatively during their sleep.
NCT Number: NCT01249924
Objective of the study: To determine whether Perioperative Auto-CPAP treatment prevent postoperative worsening of OSA and improve nocturnal oxygen saturation in surgical patients with moderate and severe OSA.
Looking for future studies?
Notify Me18 year–80 year
All sexes
Interventional
Not applicable
Mount Sinai Hospital, Department of Anesthesia, Toronto, Ontario, Canada
The patients will be approached by the study coordinators at the preoperative clinic. If the patient is interested in participating the study, STOP-Bang and Epworth questionnaires will be implemented to determine the risk for OSA.If the patients are classified as high risk of having OSA, they are scheduled for an overnight sleep study at home. The patients with Apnea-Hypopnea Index (AHI)>15 from the sleep study will be randomized into two study groups: Perioperative CPAP group or control group (routine care). In the perioperative CPAP group, patients will be treated with auto-CPAP for 2-3 nights preoperatively and 5 nights postoperatively. All patients will undergo sleep study on the third postoperative night and be monitored by a pulse oximeter for 2-3 nights preoperatively and 5 nights postoperatively.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
the patients who meet the following criteria will be recruited
Exclusion criteria
Patients will be treated with auto-CPAP preoperatively for 2-3 nights preoperatively and 5 nights postoperatively during their sleep.
Patients in this group will receive routine care, undergo sleep study on the third postoperative night and be monitored by a pulse oximeter for oxygen saturation level for 2-3 nights preoperatively and 5 nights postoperatively during their sleep.
Time frame: On the third night after surgery
Apnea-hypopnea index.
Time frame: 2-3 nights before surgery and 5 nights after surgery
Nocturnal oxygen desaturation index (ODI) and percentage of time with SaO2<90%(CT90).
Looking for future studies?
Notify MeUniversity Health Network, Toronto
Other
The Effectiveness of Perioperative CPAP to Reduce the Occurrence of Sleep Apnea Related Adverse Events in Surgical Patients With Obstructive Sleep Apnea
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07798518
Apnea, Dyssomnias
Istanbul, Turkey (Türkiye)
View Trial DetailsNCT07778121
Apnea, Diabetes Mellitus
Køge, Denmark
View Trial DetailsNCT00945776
Apnea, Dyssomnias
Charleston, West Virginia, United States
View Trial DetailsNCT03018912
Apnea, Chronobiology Disorders
Fontana, California, United States
View Trial Details