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Controlled Trial to Demonstrate a Reduction in the Number of Oliguria Events in Patients Being Managed in a Critical Care Unit, Following Cardiac Surgery, When a Novel Oliguria Prediction Tool (STABILITY UO) is Used to Identify Patients at Risk, Compared to Standard of Care.

Primary Purpose

Acute Kidney Injury

Status
Not yet recruiting
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Stability UO
Sponsored by
Rinicare Ltd
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Acute Kidney Injury

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Patient is willing and able to give informed consent for participation in the study, including being able to receive study materials at least 24 hours prior to their planned operation,
  • Patient is Male or Female, aged 18 years or above,
  • Patient is due to undergo elective or urgent cardiac surgery, and who is expected to be managed on the CTCCU postoperatively,
  • In the Investigator's opinion, able and willing to comply with all study requirements.

Exclusion Criteria:

  • Patients undergoing emergency surgery (i.e surgery that has to take place in the next available theatre even if this is out of standard operating hours)
  • Patients having ventricular assist device implantation,
  • Patients receiving a heart transplant,
  • Patients who would be unable to be treated by standard of care CTCCU therapies and practices,
  • Patients who are receiving pre or intra-operative dialysis or haemofiltration.
  • Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participant at risk because of participation in the study, or may influence the result of the study, or the participant's ability to participate in the study.

Sites / Locations

  • Wythenshawe Hospital (Manchester University NHS Foundation Trust

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention Group

Control Group

Arm Description

The clinical team has access to the Stability UO software. All other care is given as standard.

Standard care given.

Outcomes

Primary Outcome Measures

Absolute Risk Reduction (ARR) of patients experiencing ≥3 oliguria events.
An oliguria event is defined as an hourly urine output of less than 0.5ml/kg/hr.

Secondary Outcome Measures

Incidence of oliguria events during post cardiac surgery CTCCU stay
An oliguria event is defined as an hourly urine output of less than 0.5ml/kg/hr.
Absolute Risk (AR), Relative Risk (RR), Relative Risk Reduction (RRR) of severe oliguria events
An severe oliguria event is defined as an hourly urine output of less than 0.3ml/kg/hr.
Median length of total stay in hospital
median length of stay in hospital
Change in post-operative serum creatinine concentration
Standard blood test to measure serum creatinine concentration (umol/L)

Full Information

First Posted
July 28, 2021
Last Updated
April 27, 2022
Sponsor
Rinicare Ltd
Collaborators
Manchester University NHS Foundation Trust
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1. Study Identification

Unique Protocol Identification Number
NCT05001503
Brief Title
Controlled Trial to Demonstrate a Reduction in the Number of Oliguria Events in Patients Being Managed in a Critical Care Unit, Following Cardiac Surgery, When a Novel Oliguria Prediction Tool (STABILITY UO) is Used to Identify Patients at Risk, Compared to Standard of Care.
Official Title
Pivotal Phase, Randomised Controlled Trial to Demonstrate a Reduction in the Number of Oliguria Events in Patients Being Managed in a Critical Care Unit, Following Cardiac Surgery, When a Novel Oliguria Prediction Tool (STABILITY UO) is Used to Identify Patients at Risk, Compared to Standard of Care.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
May 2022 (Anticipated)
Primary Completion Date
May 2023 (Anticipated)
Study Completion Date
June 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Rinicare Ltd
Collaborators
Manchester University NHS Foundation Trust

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
Acute kidney injury (AKI) is experienced by 12% of patients following surgery and in up to 50% of patients following cardiac surgery. It is associated with an increased risk of death and prolonged stay in critical care after surgery. In addition to the patient impact, AKI costs the NHS alone between £434m and £620m per year. One way that AKI is diagnosed is by looking at a patient's urine output and checking how much is produced over time. If this value is too low for a patient, they are diagnosed with oliguria. Too many of these oliguria events leads to a diagnosis of AKI. The product to be tested (Stability UO) aims to reduce the number of patients who suffer three or more oliguria events after surgery by processing the data entered by the care team and providing the care team with additional information about the patient's risk of oliguria over the next six hours. Patients over 18 who present at Manchester University NHS Foundation Trust for non-emergency cardiac surgery will be screened and asked to consent to be randomised as part of the trial. Patients undergoing certain operations and those with unsuitable medical history (e.g. patients being treated for dialysis) will not be invited to participate. The randomisation will determine if their care team has access to the Stability UO software after surgery. While the care team looks after the patients in the cardiothoracic critical care unit (CTCCU) after surgery, they will enter that the patient's weight and amount of urine passed each hour into the software and review the output. The primary questions the study will answer is if there is a difference between number of oliguria events between the two groups of patients. The study is funded by the device manufacturer: Rinicare Ltd.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Kidney Injury

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
362 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention Group
Arm Type
Experimental
Arm Description
The clinical team has access to the Stability UO software. All other care is given as standard.
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
Standard care given.
Intervention Type
Device
Intervention Name(s)
Stability UO
Intervention Description
STABILITY UO is a standalone software, based on a Bayesian model, which quantifies the risk of an individual patient developing severe oliguria (0.3mg/kg/hr for 6 hours). The model identifies at risk patients by predicting future urine output, using only previously recorded urine output values for that individual, allowing clinicians to see the predicted risk of a patient developing severe oliguria in real time.
Primary Outcome Measure Information:
Title
Absolute Risk Reduction (ARR) of patients experiencing ≥3 oliguria events.
Description
An oliguria event is defined as an hourly urine output of less than 0.5ml/kg/hr.
Time Frame
post cardiac surgery CTCCU stay (average 2-5 days with some staying more than 3 months)
Secondary Outcome Measure Information:
Title
Incidence of oliguria events during post cardiac surgery CTCCU stay
Description
An oliguria event is defined as an hourly urine output of less than 0.5ml/kg/hr.
Time Frame
post cardiac surgery CTCCU stay (average 2-5 days with some staying more than 3 months)
Title
Absolute Risk (AR), Relative Risk (RR), Relative Risk Reduction (RRR) of severe oliguria events
Description
An severe oliguria event is defined as an hourly urine output of less than 0.3ml/kg/hr.
Time Frame
post cardiac surgery CTCCU stay (average 2-5 days with some staying more than 3 months)
Title
Median length of total stay in hospital
Description
median length of stay in hospital
Time Frame
post cardiac surgery CTCCU stay (average 2-5 days with some staying more than 3 months)
Title
Change in post-operative serum creatinine concentration
Description
Standard blood test to measure serum creatinine concentration (umol/L)
Time Frame
post cardiac surgery CTCCU stay (average 2-5 days with some staying more than 3 months)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patient is willing and able to give informed consent for participation in the study, including being able to receive study materials at least 24 hours prior to their planned operation, Patient is Male or Female, aged 18 years or above, Patient is due to undergo elective or urgent cardiac surgery, and who is expected to be managed on the CTCCU postoperatively, In the Investigator's opinion, able and willing to comply with all study requirements. Exclusion Criteria: Patients undergoing emergency surgery (i.e surgery that has to take place in the next available theatre even if this is out of standard operating hours) Patients having ventricular assist device implantation, Patients receiving a heart transplant, Patients who would be unable to be treated by standard of care CTCCU therapies and practices, Patients who are receiving pre or intra-operative dialysis or haemofiltration. Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participant at risk because of participation in the study, or may influence the result of the study, or the participant's ability to participate in the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Eric D Carlson, MRes
Phone
+44 (0)1615 37 59 29
Email
eric@rinicare.com
First Name & Middle Initial & Last Name or Official Title & Degree
Stuart Grant, PhD
Phone
+44 (0)1615 37 59 29
Email
stuart.grant@rinicare.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Roberto Mosca, MD
Organizational Affiliation
Manchester University NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Wythenshawe Hospital (Manchester University NHS Foundation Trust
City
Manchester
State/Province
Greater Manchester
ZIP/Postal Code
M23 9LT
Country
United Kingdom
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Juliette Novasio, Ph.D
Phone
0161 291 5773
Email
juliette.novasio@mft.nhs.uk
First Name & Middle Initial & Last Name & Degree
Roberto Mosca, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31663925
Citation
Howitt SH, Oakley J, Caiado C, Goldstein M, Malagon I, McCollum C, Grant SW. A Novel Patient-Specific Model for Predicting Severe Oliguria; Development and Comparison With Kidney Disease: Improving Global Outcomes Acute Kidney Injury Classification. Crit Care Med. 2020 Jan;48(1):e18-e25. doi: 10.1097/CCM.0000000000004074.
Results Reference
background
PubMed Identifier
29940876
Citation
Howitt SH, Grant SW, Caiado C, Carlson E, Kwon D, Dimarakis I, Malagon I, McCollum C. The KDIGO acute kidney injury guidelines for cardiac surgery patients in critical care: a validation study. BMC Nephrol. 2018 Jun 25;19(1):149. doi: 10.1186/s12882-018-0946-x.
Results Reference
background

Learn more about this trial

Controlled Trial to Demonstrate a Reduction in the Number of Oliguria Events in Patients Being Managed in a Critical Care Unit, Following Cardiac Surgery, When a Novel Oliguria Prediction Tool (STABILITY UO) is Used to Identify Patients at Risk, Compared to Standard of Care.

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