Status:
COMPLETED
Intraoperative Implementation of the Hypotension Probability Indicator
Lead Sponsor:
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Conditions:
Intraoperative Hypotension
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
Reducing intraoperative hypotension using FlotracIQ with HPI software.
Detailed Description
Intraoperative hypotension occurs often. Even short durations of hypotension are suggested to be associated with increased risk for renal insufficiency and myocardial ischemia. Currently treatment of ...
Eligibility Criteria
Inclusion
- Aged 18 years or older
- Planned for elective non-cardiac non-day surgery with an expected duration of more than 2 hours
- Planned to receive general anaesthesia
- Planned to receive an arterial line during surgery
- Aim for MAP of 65 mmHg during surgery
- Being able to give written informed consent prior to surgery
Exclusion
- Aim for MAP other than 65 mmHg at discretion treating physician
- Significant hypotension before surgery defined as a MAP \<65
- Right- or left sided cardiac failure (e.g. LVEF\<35%)
- Known cardiac shunts (significant)
- Known aortic stenosis (severe)
- Severe cardiac arrhythmias including atrial fibrillation
- Requiring dialysis
- Liver surgery
- Vascular surgery with clamping of the aorta
- Perioperative Goal Directed Therapy (PGDT) protocol
Key Trial Info
Start Date :
November 8 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 20 2019
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT03376347
Start Date
November 8 2017
End Date
March 20 2019
Last Update
January 13 2020
Active Locations (1)
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1
Academic Medical Center Amsterdam
Amsterdam, Netherlands