Preoperative risk estimation for onco-geriatric patients.
Suspended
- Conditions
- Surgical oncologyElderly
- Registration Number
- NL-OMON29384
- Lead Sponsor
- o sponsors
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Suspended
- Sex
- Not specified
- Target Recruitment
- 362
Inclusion Criteria
Patients aged >70 years undergoing elective surgery for a solid tumour under general anaesthesia will be included for this study.
- Patients will be stratified according to tumour localisation: intra cavity (e.g. colorectal, gynaecological) vs superficial (e.g. breast, head & neck, melanoma).
Exclusion Criteria
- Patients not able to give informed consent
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method - Primary endpoint will be 30 day morbidity and mortality.
- Secondary Outcome Measures
Name Time Method - Secondary endpoints will be length of hospital stay and the number of additional specialists involved in patient care in the 30 days after surgery.