Hypotension Decision Assist - Use, Safety and Efficacy (HDA-USE)
Primary Purpose
Intraoperative Hypotension
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Monitored by HDA
Sponsored by
About this trial
This is an interventional prevention trial for Intraoperative Hypotension focused on measuring Hypotension, Intraoperative care, Intraoperative complications
Eligibility Criteria
Inclusion Criteria:
- Adults (≥18 years) due to undergo elective surgery who are likely to have an arterial line sited as part of their standard intraoperative care.
- Recruitment after booking for surgery with sufficient time to read, understand and question study patient information prior to attending for surgery.
- Ability and willingness to provide informed consent
- Expected duration of anaesthesia > 60 minutes
- Intra-arterial monitoring is part of routine clinical care
Exclusion Criteria:
- Inability to provide informed consent
- No arterial line planned as part of their intraoperative care
- Aged < 18 years of age
- Patients with aortic regurgitation
- Patients fitted with an intra-aortic balloon pump (IABP)
- No other intra-arterial pressure management system in use
- Concurrent participation in another experimental intervention or drug study
Sites / Locations
- Queen Elizabeth Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Monitored with HDA
Arm Description
Participants undergoing elective major surgery and have an arterial line as part of their standard care with HDA included as part of their care
Outcomes
Primary Outcome Measures
Display of trends in mean arterial pressure measured in millimetres of mercury (mmHg)
Operative time were HDA derives and displays mean arterial pressure (mmHg) data that is relevant to the management of the blood pressure, hemodynamic stability and the cardiovascular system of the patient.
Display of trends in systolic blood pressure measured in millimetres of mercury (mmHg)
Operative time were HDA derives and displays systolic blood pressure (mmHg) data that is relevant to the management of the blood pressure, hemodynamic stability and the cardiovascular system of the patient.
Display of trends in diastolic blood pressure measured in millimetres of mercury (mmHg)
Operative time were HDA derives and displays diastolic blood pressure (mmHg) data that is relevant to the management of the blood pressure, hemodynamic stability and the cardiovascular system of the patient.
Display of trends in heart rate measured in beats per minute (bpm)
Operative time were HDA derives and displays heart rate (bpm) data that is relevant to the management of the blood pressure, hemodynamic stability and the cardiovascular system of the patient.
Display of trends of changes in heart rate (percentage) over the previous five minutes measured as a percentage
Operative time were HDA derives and displays changes in heart rate (percentage) data that is relevant to the management of the blood pressure, hemodynamic stability and the cardiovascular system of the patient.
Display of trends of changes in cardiac output (percentage) over the previous five minutes measured as a percentage
Operative time were HDA derives and displays changes in cardiac output (percentage) data that is relevant to the management of the blood pressure, hemodynamic stability and the cardiovascular system of the patient.
Display of trends of changes in systemic vascular resistance (percentage) over the previous five minutes measured as a percentage
Operative time were HDA derives and displays changes in systemic vascular resistance (percentage) data that is relevant to the management of the blood pressure, hemodynamic stability and the cardiovascular system of the patient.
Adverse events (AEs) related to blood pressure attributable to HDA
Incidence, severity and causality of all AEs with delineation of those that are attributable to the use of HDA
Secondary Outcome Measures
Measurement of intraoperative hypotension
Measured incidence of Mean Arterial Pressure < 65 for at least 1 minute
Number and type of intervention made by anaesthetists
Quantification of interventions related to patient cardiovascular management including fluid administered, cardiovascular active drugs administered and or drug infusion rate changes if applicable
Comparison of HDA projected trend feature
Comparison of the estimated MAP at +2mins by projected trend feature versus the observed Mean Arterial Pressure at that time as it arises.
Anaesthetists evaluation of use against a five point Likert-type scale
Anaesthetists evaluation of the ease of use and usefulness of HDA ranked in accordance with a five-point Likert-type rating scale where the minimum value is 1 (strongly disagree that HDA is useful or easy to use) and the maximum is 5 (strongly agree that HDA is useful or easy to use) .
Full Information
NCT ID
NCT05101590
First Posted
October 1, 2021
Last Updated
March 21, 2022
Sponsor
Directed Systems Limited
Collaborators
University Hospital Birmingham NHS Foundation Trust, Innovate UK
1. Study Identification
Unique Protocol Identification Number
NCT05101590
Brief Title
Hypotension Decision Assist - Use, Safety and Efficacy
Acronym
HDA-USE
Official Title
A Study of the Use, Safety and Efficacy of the Hypotension Decision Assist Device
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
October 22, 2021 (Actual)
Primary Completion Date
February 28, 2022 (Actual)
Study Completion Date
February 28, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Directed Systems Limited
Collaborators
University Hospital Birmingham NHS Foundation Trust, Innovate UK
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This clinical investigation will investigate whether Hypotension Decision Assist (HDA) is a feasible, safe and effective patient clinical decision support system to enhance an anaesthetist's ability to manage a patient's cardiovascular system when undergoing surgery. If successful, this study will provide evidence that the use of HDA facilitates beneficial outcomes for patients who have this device used.
Detailed Description
In this study participants who are due to undergo elective major surgery and have an arterial line as part of their standard care will be invited to have the additional monitoring device (HDA) included as part of their care. Agreeing participants will have demographic, contact and medical history information necessary to conduct the study recorded, including a record of their intraoperative arterial line measurements.
After completing the consent process participants will receive intraoperative monitoring with Hypotension Decision Assist in addition to their standard care. The HDA monitor will be attached to the patient vital signs monitor, which will in turn be attached to the blood pressure transducer. All sampled arterial line data collected by the patient vital signs monitored will be automatically transmitted in real time to the HDA device via a serial cable attached to a digital export port of the vital signs monitor. HDA will process this input data to display, in graphical and numeric format, vital signs data and physiological parameters derived from the arterial wave form data including: Mean Arterial Pressure (MAP), systolic and diastolic blood pressure, heart rate and changes in heart rate, cardiac output and systemic vascular resistance.
The output from the study will be compared to the primary and secondary outcomes to evaluate the performance and safety of the device and to evaluate whether HDA improves control of the cardiovascular system from the anaesthetists' perspective.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Intraoperative Hypotension
Keywords
Hypotension, Intraoperative care, Intraoperative complications
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Monitored with HDA
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Monitored with HDA
Arm Type
Experimental
Arm Description
Participants undergoing elective major surgery and have an arterial line as part of their standard care with HDA included as part of their care
Intervention Type
Device
Intervention Name(s)
Monitored by HDA
Intervention Description
Participants undergoing elective major surgery with an arterial line as part of their standard care and additional monitoring with HDA as part of their care.
Primary Outcome Measure Information:
Title
Display of trends in mean arterial pressure measured in millimetres of mercury (mmHg)
Description
Operative time were HDA derives and displays mean arterial pressure (mmHg) data that is relevant to the management of the blood pressure, hemodynamic stability and the cardiovascular system of the patient.
Time Frame
Intraoperative
Title
Display of trends in systolic blood pressure measured in millimetres of mercury (mmHg)
Description
Operative time were HDA derives and displays systolic blood pressure (mmHg) data that is relevant to the management of the blood pressure, hemodynamic stability and the cardiovascular system of the patient.
Time Frame
Intraoperative
Title
Display of trends in diastolic blood pressure measured in millimetres of mercury (mmHg)
Description
Operative time were HDA derives and displays diastolic blood pressure (mmHg) data that is relevant to the management of the blood pressure, hemodynamic stability and the cardiovascular system of the patient.
Time Frame
Intraoperative
Title
Display of trends in heart rate measured in beats per minute (bpm)
Description
Operative time were HDA derives and displays heart rate (bpm) data that is relevant to the management of the blood pressure, hemodynamic stability and the cardiovascular system of the patient.
Time Frame
Intraoperative
Title
Display of trends of changes in heart rate (percentage) over the previous five minutes measured as a percentage
Description
Operative time were HDA derives and displays changes in heart rate (percentage) data that is relevant to the management of the blood pressure, hemodynamic stability and the cardiovascular system of the patient.
Time Frame
Intraoperative
Title
Display of trends of changes in cardiac output (percentage) over the previous five minutes measured as a percentage
Description
Operative time were HDA derives and displays changes in cardiac output (percentage) data that is relevant to the management of the blood pressure, hemodynamic stability and the cardiovascular system of the patient.
Time Frame
Intraoperative
Title
Display of trends of changes in systemic vascular resistance (percentage) over the previous five minutes measured as a percentage
Description
Operative time were HDA derives and displays changes in systemic vascular resistance (percentage) data that is relevant to the management of the blood pressure, hemodynamic stability and the cardiovascular system of the patient.
Time Frame
Intraoperative
Title
Adverse events (AEs) related to blood pressure attributable to HDA
Description
Incidence, severity and causality of all AEs with delineation of those that are attributable to the use of HDA
Time Frame
Intraoperative
Secondary Outcome Measure Information:
Title
Measurement of intraoperative hypotension
Description
Measured incidence of Mean Arterial Pressure < 65 for at least 1 minute
Time Frame
Intraoperative
Title
Number and type of intervention made by anaesthetists
Description
Quantification of interventions related to patient cardiovascular management including fluid administered, cardiovascular active drugs administered and or drug infusion rate changes if applicable
Time Frame
Intraoperative
Title
Comparison of HDA projected trend feature
Description
Comparison of the estimated MAP at +2mins by projected trend feature versus the observed Mean Arterial Pressure at that time as it arises.
Time Frame
Intraoperative
Title
Anaesthetists evaluation of use against a five point Likert-type scale
Description
Anaesthetists evaluation of the ease of use and usefulness of HDA ranked in accordance with a five-point Likert-type rating scale where the minimum value is 1 (strongly disagree that HDA is useful or easy to use) and the maximum is 5 (strongly agree that HDA is useful or easy to use) .
Time Frame
Intraoperative
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adults (≥18 years) due to undergo elective surgery who are likely to have an arterial line sited as part of their standard intraoperative care.
Recruitment after booking for surgery with sufficient time to read, understand and question study patient information prior to attending for surgery.
Ability and willingness to provide informed consent
Expected duration of anaesthesia > 60 minutes
Intra-arterial monitoring is part of routine clinical care
Exclusion Criteria:
Inability to provide informed consent
No arterial line planned as part of their intraoperative care
Aged < 18 years of age
Patients with aortic regurgitation
Patients fitted with an intra-aortic balloon pump (IABP)
No other intra-arterial pressure management system in use
Concurrent participation in another experimental intervention or drug study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thomas Clutton-Brock
Organizational Affiliation
University Hospital Birmingham NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Queen Elizabeth Hospital
City
Birmingham
ZIP/Postal Code
B15 2TH
Country
United Kingdom
12. IPD Sharing Statement
Plan to Share IPD
No
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Hypotension Decision Assist - Use, Safety and Efficacy
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