Biomarker Use in Evidence of Neuronal Damage in Response to Anaesthesia and Surgery (The BOUNDARY Study)
- Conditions
- DeliriumPostoperative Cognitive DysfunctionAnaesthesiology - AnaestheticsNeurological - DementiasSurgery - Other surgery
- Registration Number
- ACTRN12620000101987
- Lead Sponsor
- St Vincent's Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 118
1. 65 years of age
2. Scheduled for elective non-cardiac surgery
3. Undergoing a procedure equally suited to intravenous (TIVA) or volatile anaesthetic management
4. Have no contraindication to neuropsychological testing (e.g. language, visual or hearing impairment)
5. Reside in an accessible proximity to the hospital for neuropsychological testing
1. Pre-existing neurological or clinically evident neurovascular disease (e.g. stroke)
2. Dementia of any aetiology
3. Received a general anaesthetic in previous 6 months
4. Associated medical problems that may lead to significant complications and loss to follow-up
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method