The effect of proactive versus reactive treatment of hypotension on postoperative disability and outcome
- Conditions
- Intraoperative hypotension, postoperative disability and outcome
- Registration Number
- NL-OMON25882
- Lead Sponsor
- niversity Medical Center Utrecht, The Netherlands
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 5000
In order to be eligible to participate in this study, a subject must meet all of the following criteria:
•Adult =18 years or older
•Elective, non-cardiac surgery under general anaesthesia or central neuraxial anaesthesia
•Expected hospital stay of at least one night after surgery
A potential subject who meets any of the following criteria will be excluded from participation in this study:
•Low risk surgery: Opthalmic surgery, endoscopic gastrointestinal procedures, (interventional) radiologic procedures, obstetric procedure
•Organ transplantation
•Procedures with a scheduled surgical time of less than 30 minutes
•Participation in another clinical trial that is interfering with the procedures and outcomes of the PRETREAT trial
•Patients unable to fully comply to study needs (e.g. legally incapable patients or patients unable to communicate in Dutch or English).
•Patients with an American Society of Anaesthesiologists (ASA) Physical status 5
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method