The Integrated Pulmonary Index (IPI) for assessment of the postoperative respiratory conditio
- Conditions
- Postoperative conditionRespirationMonitoringPostoperatieve conditieAdemhalingMonitoring
- Registration Number
- NL-OMON28414
- Lead Sponsor
- MC
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
Adult (> 17 years) ASA 1-3 patients that underwent elective surgery under general anesthesia who require opioid pain relief and are able to wear or retain the IPI device post-operatively.
Exclusion Criteria
Patients having ENT, facial or neurological/ brain (head) surgery or are not able to give informed consent.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The function of the IPI monitor and the number of IPI-events during the first day and night after after anesthesia and the use of opiods (ie. number of IPI events, IPI AUC) are the main end-points.
- Secondary Outcome Measures
Name Time Method