An observational study measuring respiratory rate as assessed by respiR8® in post operative patients aged 60 years and above

Completed

• Conditions: postoperatieve monitoring; postoperative breathing monitoring

• Registration Number: NL-OMON40777
• Lead Sponsor: eids Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 50

Inclusion Criteria

• Males and females having elective surgery
• Having surgery requiring anaesthesia for at least 60 minutes
• Aged >= 60 years
• Expected to stay in hospital for at least 12 hours
• General Anaesthesia / regional anaesthesia
• Able to read and understand the English or Dutch Patient Information Leaflet and Consent Form.

Exclusion Criteria

• Head, neck and facial surgery
• Inability to wear or retain a standard oxygen mask post-operatively
• Emergency (non-elective) surgery

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Breathing frequency</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Oxygen saturation</p><br>