Non-invasive Measurement of the Hypotension Prediction Index for the Reduction of Intraoperative Hypotension
Clearsight
Prospective Interventional Study Investigating a Goal-directed Therapy Based on Non-invasive Measurement of the Hypotension Prediction Index for the Reduction of Hypotension in Patients Undergoing Major Orthopedic and Trauma Surgery
1 other identifier
interventional
150
1 country
1
Brief Summary
In order to reduce the incidence of IOH, various goal-directed therapy (GDT) protocols have already been introduced with success regarding the reduction of postoperative AKI and MINS. However, these studies used an invasive hemodynamic monitoring which offered a continuous surveillance of the blood pressure. In contrast, standard non-invasive blood pressure monitoring results in a blind gap between two measurements (mostly three or five minutes). In order to address this limitation, different continuous non-invasive blood pressure monitoring devices have been introduced. The next evolutional step of non-invasive cardiac output monitoring was to prevent IOH before their onset by using the Hypotension Prediction Index (HPI). Based on the Edward ́s monitoring platform, HPI is a monitoring tool which aims to predict IOH (defined as MAP\<65 mmHg for at least one minute) up to 15 min before its onset. The underlying machine learning based algorithm uses analyses features from the pressure waveform and was first calculated from a large retrospective data set of surgical patients and subsequently validated in a prospective cohort. In this study HPI showed a sensitivity of 88% and specificity of 87% for predicting IOH 15 min before its onset. Since then, own and studies of other working groups confirmed the effective prevention of IOH by the use of HPI-based GDT. Until today the arterial waveform analysis was dependent on invasive arterial measurement but since Edwards Lifesciences already promoted the start of the HPI on the ClearSight platform a non-invasive measurement will soon be possible. Further, until now it has not yet been proven that the perioperative use of a continuous non-invasive blood pressure monitoring has a beneficial effect on the patient´s outcome. Study objectives The aim of the study is to investigate whether a hemodynamic protocol based on continuous non-invasive cardiac output monitoring (ClearSight system) compared to standard care can reduce the incidence of IOH, postoperative AKI, and MINS in patients undergoing major trauma and orthopedic surgery.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Aug 2024
1 active site
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Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 15, 2024
CompletedFirst Posted
Study publicly available on registry
March 4, 2024
CompletedStudy Start
First participant enrolled
August 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
March 31, 2026
CompletedApril 3, 2025
March 1, 2025
8 months
February 15, 2024
March 31, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Change of the frequency of intraoperative hypotension
Change of the frequency of intraoperative hypotension (defined as MAP below 65mmHg, frequency ((n)/h)
through study completion, an average of 1 year
Change of the absolute duration of of intraoperative hypotension
Change of the absolute duration of intraoperative hypotension (defined as MAP below 65mmHg, unit: minutes)
through study completion, an average of 1 year
Change of the relative duration of intraoperative hypotension
Change of the relative duration of intraoperative hypotension (defined as MAP below 65mmHg, unit: percentage of total anesthesia time)
through study completion, an average of 1 year
Secondary Outcomes (2)
AKI
through study completion, an average of 1 year
MINS
through study completion, an average of 1 year
Study Arms (2)
Interventional group
ACTIVE COMPARATORGDT-therapy guided hemodynamic management based on Clearsight system
Control group
NO INTERVENTIONClearsight-monitor is blinded but records standard hemodynamic care
Interventions
Intraoperative use of a HPI-guided hemodynamic goal-directed protocol based on the non-invasive measurement of HPI (Clearsight system)
Eligibility Criteria
You may qualify if:
- Patients undergoing major trauma or orthopedic surgery in supine position, which is defined as:
- Reconstructive Surgery of the pelvis (e.g., stabilization of fractures)
- Total hip arthroplasty
- Surgery of the proximal femur (e.g., stabilization of fractures)
- Total knee arthroplasty
- Surgery of the spine
- Performance of general anesthesia with planned duration of \>90min
- Age ≥ 45 years
You may not qualify if:
- Planned invasive blood pressure monitoring
- Participation in another interventional study
- Pregnancy and nursing mothers
- Surgery without controlled mechanical ventilation
- ASA I or IV
- Arterial Fibrillation
- Allergy against gelantine
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Giessenlead
- Edwards Lifesciencescollaborator
Study Sites (1)
Justus-Liebig-University of Giessen
Giessen, 35392, Germany
Related Publications (42)
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PMID: 41168839DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Michael Sander, Prof.
Justus-Liebig-University of Giessen
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, CARE PROVIDER
- Masking Details
- All patients are connected to the Clearsight device but the interface is masked in the control group.
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 15, 2024
First Posted
March 4, 2024
Study Start
August 1, 2024
Primary Completion
March 31, 2025
Study Completion
March 31, 2026
Last Updated
April 3, 2025
Record last verified: 2025-03
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF, CSR, ANALYTIC CODE
- Time Frame
- The study data can be checked on reasonable request by contact the PI after the end of the analysis (appr. after 06/2025). The study protocol, SAP, ICF can been assessed after the start of the study.
- Access Criteria
- The data can be accessed by writing an email to the PI. He checks the if the request is reasonable (e.g., for review purpose) and will then provide the information per mail.
The study data can be checked on reasonable request by contact the PI.