Continuous Finger-cuff Arterial Pressure Monitoring and Intraoperative Hypotension During Non-cardiac Surgery: the Randomized DETECT II Trial
Not Applicable
Recruiting
- Conditions
- Intraoperative Hypotension
- Registration Number
- NCT06753097
- Lead Sponsor
- Universitätsklinikum Hamburg-Eppendorf
- Brief Summary
This is a randomized trial (1) investigating whether continuous finger-cuff - compared to intermittent oscillometric - arterial pressure monitoring reduces the amount of intraoperative hypotension (specifically, from the start of induction of general anesthesia until the end of surgery) in low-to-moderate risk patients having elective non-cardiac surgery.
- Detailed Description
not provided
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 930
Inclusion Criteria
Not provided
Exclusion Criteria
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Time-weighted average mean arterial pressure <65 mmHg during the start of induction of general anesthesia until the end of surgery
- Secondary Outcome Measures
Name Time Method Time-weighted average mean arterial pressure <60 mmHg during the start of induction of general anesthesia until the end of surgery Time-weighted average mean arterial pressure <50 mmHg during the start of induction of general anesthesia until the end of surgery Time-weighted average mean arterial pressure <40 mmHg during the start of induction of general anesthesia until the end of surgery Absolute number of patients with at least one 1-minute episode of a mean arterial pressure <65 mmHg during the start of induction of general anesthesia until the end of surgery Absolute number of patients with at least one 1-minute episode of a mean arterial pressure <60 mmHg during the start of induction of general anesthesia until the end of surgery Absolute number of patients with at least one 1-minute episode of a mean arterial pressure <50 mmHg during the start of induction of general anesthesia until the end of surgery Absolute number of patients with at least one 1-minute episode of a mean arterial pressure <40 mmHg during the start of induction of general anesthesia until the end of surgery Cumulative duration of a mean arterial pressure <65 mmHg during the start of induction of general anesthesia until the end of surgery Time-weighted average mean arterial pressure >100 mmHg during the start of induction of general anesthesia until the end of surgery Time-weighted average mean arterial pressure >110 mmHg during the start of induction of general anesthesia until the end of surgery Time-weighted average mean arterial pressure >120 mmHg during the start of induction of general anesthesia until the end of surgery Time-weighted average mean arterial pressure >140 mmHg during the start of induction of general anesthesia until the end of surgery
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
How does continuous finger-cuff monitoring in DETECT II (NCT06753097) compare to intermittent oscillometric methods in reducing intraoperative hypotension during non-cardiac surgery?
What adverse events are associated with continuous finger-cuff arterial pressure monitoring versus standard intermittent methods in the DETECT II trial?
Are there patient-specific biomarkers or risk factors that predict response to continuous arterial pressure monitoring in non-cardiac surgical settings?
How does the DETECT II trial's approach to hypotension monitoring compare with other real-time blood pressure technologies in clinical practice?
What are the long-term postoperative outcomes in patients using continuous finger-cuff monitoring versus standard methods in the DETECT II trial?
Trial Locations
- Locations (1)
University Medical Center Hamburg-Eppendorf
🇩🇪Hamburg, Germany