NL-OMON25882RecruitingNot Applicable
The effect of proactive versus reactive treatment of hypotension on postoperative disability and outcome in surgical patients under anaesthesia (PRETREAT): an adaptive, multicentre randomized controlled trial
niversity Medical Center Utrecht, The Netherlands0 sites5,000 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- Enrollment
- 5,000
Study Overview
Brief Summary
/A
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •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
Exclusion Criteria
- •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
Investigators
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