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Hemodynamic OptimizaTion in Sitting POsition Surgery Trial (HOTSPOT)

Primary Purpose

Hemodynamic Instability, Blood Pressure, Low, Orthopedic Disorder

Status
Recruiting
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
ClearSight
Sponsored by
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hemodynamic Instability

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

1. patients candidate for elective orthopedic surgery in sitting position under general anesthesia + interscalene block

Exclusion Criteria:

  1. non-elective patients (acute trauma) and hemodynamically unstable patients
  2. vascular system pathologies
  3. pregnant women
  4. patient refusal to participate to the study

Sites / Locations

  • Policlinico A. GemelliRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Intermittent NIBP monitoring

ClearSight

Arm Description

Oscillometric intermittent (3 mins) noninvasive blood pressure monitoring

Continuous non invasive hemodynamic monitoring

Outcomes

Primary Outcome Measures

TWA MAP < 65 mmhg (expressed in mmHg)
The measure of hypotension will be expressed with the TWA-MAP value (time-weighted average intraoperative MAP) in mmHg to define the severity and duration of the hypotensive episode. The TWA MAP under a threshold of 65 mmHg will be calculated as the area between 65 mmHg threshold and the curve of the MAP measurements divided by total continuous reading time in minutes.

Secondary Outcome Measures

Rate of severe hypotensive episodes (MAP <60 mmHg or <50 mmHg)
The number of severe hypotensive episodes (MAP <60 mmHg or <50 mmHg) recorded.
Time to event (in seconds)
How long does it take for the medical staff to correct the hypotensive episode (in seconds).
Quantity of vasopressors and/or fluids
Quantity of vasopressors (expressed in mg) and/or fluids (expressed in ml) used to correct the hypotensive events.
Incidence of perioperative adverse cardiac events.
Major Adverse Cardiovascular Events - MACE - will be defined, according to the 3 points MACE, as a composite of non fatal stroke, non fatal myocardial infarction and cardiovascular death occurred within 30 postoperative days.
Incidence of perioperative acute kidney injury.
Acute Kidney Iniury - AKI - will be defined, according to the KDIGO criteria, as an increase in serum creatinine by greather than or equal to 0.3 mg/dL within 48 postoperative hours.

Full Information

First Posted
November 10, 2021
Last Updated
October 19, 2023
Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
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1. Study Identification

Unique Protocol Identification Number
NCT05143632
Brief Title
Hemodynamic OptimizaTion in Sitting POsition Surgery Trial
Acronym
HOTSPOT
Official Title
Continuous Non-invasive Blood Pressure Monitoring to Increase Hemodynamic Stability During Sitting Position Orthopedic Surgery: Prospective Randomized Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 28, 2022 (Actual)
Primary Completion Date
July 30, 2024 (Anticipated)
Study Completion Date
December 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
Intraoperative hypotension (MAP <65 mmHg) in patients undergoing general anesthesia is a notable risk factor for the development of post-operative complications including acute kidney injury (AKI), myocardial injury, stroke and delirium, and is strongly associated with increased mortality. Moreover, the mean and systolic blood pressure values tend to undergo significant fluctuations with different positions assumed by the patient during surgery. Since severe hypotensive phenomena are connected with cerebral hypoperfusion and are associated with negative outcomes, close monitoring of blood pressure is necessary. The primary endpoint of this study is to evaluate the number of hypotensive episodes, their quality and their duration in patients monitored with the oscillometric intermittent noninvasive blood pressure method compared to patients with continuous noninvasive monitoring using ClearSight during orthopedic surgery in sitting position performed under general anesthesia and with interscalene block. The measure of hypotension will be expressed (in mmHg) with the TWA-MAP value (time-weighted average intraoperative MAP) to define the severity and duration of the hypotensive episode. For a subgroup of patients, brain oximetry will be monitored using the ForeSight system to record episodes of cerebral desaturation. Secondary endpoints include: number of severe hypotensive episodes (MAP <60 mmHg or <50 mmHg) recorded; time to event: how long does it take for the medical staff to correct the hypotensive episode (treated according to the planned protocol); quantity of vasopressors and/or fluids used to correct the hypotensive event; incidence of perioperative adverse cardiac events and acute kidney injury. The primary hypothesis is that continuous non-invasive monitoring using ClearSight reduces the incidence of intraoperative hypotensive events (defined by mean arterial pressure below a value of 65 mmHg for more than 1 minute) and the duration of the events themselves, leading to an improvement in patients' outcomes.
Detailed Description
Intraoperative hypotension (MAP <65 mmHg) in patients undergoing general anesthesia is a notable risk factor for the development of post-operative complications including acute kidney injury (AKI), myocardial injury, stroke and delirium, and is strongly associated with increased mortality. Moreover, the mean and systolic blood pressure values tend to undergo significant fluctuations with different positions assumed by the patient during surgery, decreasing in the transition from the supine position to the sitting position (beach chair position) typically used during surgery that involves the anatomical district of the shoulder or proximal humerus. Since severe hypotensive phenomena are connected with cerebral hypoperfusion and are associated with negative outcomes, close monitoring of blood pressure is necessary. The investigators have introduced in clinical practice the use of non-invasive ClearSight sensor (Edwards Lifesciences Corp, Irvine CA, USA), which uses the volume-clamp and Physiocal technologies to obtain continuously calibrated blood pressure values and hemodynamic parameters. The primary endpoint of this study is to evaluate the number of hypotensive episodes, their quality and their duration in patients monitored with the oscillometric intermittent noninvasive blood pressure method compared to patients with continuous noninvasive monitoring using ClearSight during orthopedic surgery in seated position performed under general anesthesia and with interscalene block. The measure of hypotension will be expressed with the TWA-MAP value (time-weighted average intraoperative MAP) to define the severity and duration of the hypotensive episode. For a subgroup of patients, brain oximetry will be monitored using the ForeSight system to record episodes of cerebral desaturation. Secondary endpoints include: number of severe hypotensive episodes (MAP <60 mmHg or <50 mmHg) recorded; time to event: how long does it take for the medical staff to correct the hypotensive episode (treated according to the planned protocol); quantity of vasopressors and/or fluids used to correct the hypotensive event; incidence of perioperative adverse cardiac events and acute kidney injury. The primary hypothesis is that continuous non-invasive monitoring using ClearSight reduces the incidence of intraoperative hypotensive events (defined by mean arterial pressure below a value of 65 mmHg for more than 1 minute) and the duration of the events themselves, leading to an improvement in patients' outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemodynamic Instability, Blood Pressure, Low, Orthopedic Disorder

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intermittent NIBP monitoring
Arm Type
No Intervention
Arm Description
Oscillometric intermittent (3 mins) noninvasive blood pressure monitoring
Arm Title
ClearSight
Arm Type
Experimental
Arm Description
Continuous non invasive hemodynamic monitoring
Intervention Type
Device
Intervention Name(s)
ClearSight
Intervention Description
The primary hypothesis is that continuous non-invasive monitoring using ClearSight reduces the incidence of intraoperative hypotensive events (defined by mean arterial pressure below a value of 65 mmHg for more than 1 minute) and the duration of the events themselves, leading to an improvement in patients' outcomes.
Primary Outcome Measure Information:
Title
TWA MAP < 65 mmhg (expressed in mmHg)
Description
The measure of hypotension will be expressed with the TWA-MAP value (time-weighted average intraoperative MAP) in mmHg to define the severity and duration of the hypotensive episode. The TWA MAP under a threshold of 65 mmHg will be calculated as the area between 65 mmHg threshold and the curve of the MAP measurements divided by total continuous reading time in minutes.
Time Frame
Surgery time
Secondary Outcome Measure Information:
Title
Rate of severe hypotensive episodes (MAP <60 mmHg or <50 mmHg)
Description
The number of severe hypotensive episodes (MAP <60 mmHg or <50 mmHg) recorded.
Time Frame
Surgery time
Title
Time to event (in seconds)
Description
How long does it take for the medical staff to correct the hypotensive episode (in seconds).
Time Frame
Surgery time
Title
Quantity of vasopressors and/or fluids
Description
Quantity of vasopressors (expressed in mg) and/or fluids (expressed in ml) used to correct the hypotensive events.
Time Frame
Surgery time
Title
Incidence of perioperative adverse cardiac events.
Description
Major Adverse Cardiovascular Events - MACE - will be defined, according to the 3 points MACE, as a composite of non fatal stroke, non fatal myocardial infarction and cardiovascular death occurred within 30 postoperative days.
Time Frame
30 postoperative days.
Title
Incidence of perioperative acute kidney injury.
Description
Acute Kidney Iniury - AKI - will be defined, according to the KDIGO criteria, as an increase in serum creatinine by greather than or equal to 0.3 mg/dL within 48 postoperative hours.
Time Frame
48 postoperative hours.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1. patients candidate for elective orthopedic surgery in sitting position under general anesthesia + interscalene block Exclusion Criteria: non-elective patients (acute trauma) and hemodynamically unstable patients vascular system pathologies pregnant women patient refusal to participate to the study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Vergari
Phone
+390630153288
Email
alessandro.vergari@policlinicogemelli.it
Facility Information:
Facility Name
Policlinico A. Gemelli
City
Rome
ZIP/Postal Code
00168
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alessandro Vergari
Phone
+ 39 06 3015 3288
Email
alessandro.vergari@policlinicogemelli.it

12. IPD Sharing Statement

Plan to Share IPD
No

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Hemodynamic OptimizaTion in Sitting POsition Surgery Trial

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