Surveillance of high-risk early postsurgical patients for real-time detection of complications using wireless monitoring
Recruiting
- Conditions
- Post-operatieve patienten die een intermediar of hoog-risico ingreep ondergaan en-of trauma patientencomplications after operationPostoperative complications10017998
- Registration Number
- NL-OMON49433
- Lead Sponsor
- Academisch Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 1892
Inclusion Criteria
Patients undergoing intermediate or high-risk major non-cardiac surgery at the
Academic Medical Center Amsterdam (AMC), and the University Medical Center
Utrecht (UMCU) or trauma patients
Exclusion Criteria
Inability to give written and informed consent
Patient refusal.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Disability-free survival 3 months after surgery (WHODAS 2.0, 12 items)</p><br>
- Secondary Outcome Measures
Name Time Method