Clinical efficacy of Remote continuous Monitoring supplementary to intermittent monitoring compared to intermittent monitoring on a surgical ward in a large Teaching hospital in the Netherlands
- Conditions
- surgical, gastroenterology and gynaecological oncology surgical admissions on a general ward
- Registration Number
- NL-OMON26077
- Lead Sponsor
- Albert Schweitzer Hospital, Dordrecht,
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 285
Inclusion Criteria
at least 18 years old; surgical, gastroenterology and gynaecological oncology surgical admissions; expected length of stay > 24 h; informed consent
Exclusion Criteria
An allergy to skin adhesives, wound or skin lesion near the application site, patients with a pacemaker or implantable cardioverter defibrillator, patients in a palliative trajectory, patients waiting for placement in a nursery home.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method total length of hospital stay
- Secondary Outcome Measures
Name Time Method cardiac arrests, mortality, unplanned ICU admissions, 30-day readmission, RRT calls, experience patients, experience care professionals, alarmfatigue <br>