Mobile Vital Sign tracking in high risk surgical ward patients
Recruiting
- Conditions
- pre- en postoperatieve complicatie na hoog risico chirurgieclinical deteriorationPre and postoperative complications10017998
- Registration Number
- NL-OMON46115
- Lead Sponsor
- Ziekenhuisgroep Twente
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 80
Inclusion Criteria
The study population includes two patient groups:
1. Patients aged > 18 years undergoing elective oesophageal and gastric resection admitted to the gastrointestinal surgical ward for postoperative care
2. Patients aged > 70 undergoing hip fracture surgery acutely admitted to the geriatric-trauma ward for pre- and postoperative care
Exclusion Criteria
1. Contraindications for use of vital sign sensor patch (i.e. skin allergy, implanted medical devices, contact isolation, etc.)
2. Diagnosed or suspected delirium, cognitive impairment, or dementia
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method