Preoperative risk estimation for onco-geriatric patients a clinical trial for the comparison of different preoperative assessment tools in the elderly surgical patient
Completed
- Conditions
- cancer1001799110019190
- Registration Number
- NL-OMON32521
- Lead Sponsor
- eids Universitair Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 15
Inclusion Criteria
aged > 70 years, elective surgical cancer treatment, under general anesthesia,
give written inforemd consent
Exclusion Criteria
patients requiring emergency surgical management within 24 hours
unable to give written informed consent
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Primary endpoint will be 30 day morbidity and mortality.</p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary endpoints will be length of hospital stay and the number of<br /><br>additional specialists involved in patient care in the 30 days after surgery. </p><br>