Clinical efficacy of continuous remote monitoring compared to intermittent monitoring on a surgical ward in a large European teaching hospital
- Conditions
- post-operatieve complications (rebleeding, infection, myocardial infarction etc)(post-operative) adverse eventsfailure to rescue
- Registration Number
- NL-OMON51127
- Lead Sponsor
- Albert Schweitzer Ziekenhuis
- 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 <p>The main study parameter is the total length of hospital stay </p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary endpoints: cardiac arrests, mortality, unplanned ICU admissions,<br /><br>30-day readmission, RRT calls<br /><br><br /><br>Other study parameters are age, gender, % acute admission, charlson comorbidity<br /><br>index (CCI), international classification disease (ICD), limitation of medical<br /><br>treatment (LOMT). </p><br>