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ECCO2R as an Adjunct to NIV in AECOPD

Primary Purpose

Chronic Obstructive Pulmonary Disease

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
NIV
ECCO2R
Sponsored by
Guy's and St Thomas' NHS Foundation Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Chronic Obstructive Pulmonary Disease focused on measuring Acute Exacerbation Chronic Obstructive Pulmonary Disease, AECOPD, Non invasive ventilation, NIV, Extracorporeal carbon dioxide removal, ECCO2R

Eligibility Criteria

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

Inclusion criteria

  • Known COPD with an acute exacerbation. An acute exacerbation is defined as per the GOLD criteria as an increase in dyspnoea, cough and/or sputum over the patient's normal symptoms. A severe exacerbation is defined as one requiring hospital admission.
  • Patients with a persistent arterial pH<7.30 due primarily to hypercapnic respiratory failure after standard medical therapy and at least 1 hour of NIV.
  • Age over 18

Exclusion Criteria

  • Haemodynamic instability after ensuring euvolaemia
  • Acute multiple organ failure requiring other organ supportive therapy, including indication for intubation and mechanical ventilation
  • Known allergy/intolerance of heparin including known heparin induced thrombosis and thrombocytopaenia
  • Acute uncontrolled haemorrhage
  • Intracerebral haemorrhage
  • Recent (<6 months) ischaemic cerebrovascular accident
  • Organ transplant recipient
  • Expected to die within 24 hours
  • Venous abnormality or body habitus precluding cannulation
  • Contraindication to NIV (as per British Thoracic Society recommendation)

    • Facial burns/trauma/recent facial or upper airway surgery
    • Vomiting
    • Fixed upper airway obstruction
    • Undrained pneumothorax
    • Recent upper gastrointestinal surgery
    • Inability to protect the airway
    • Life threatening hypoxaemia (PaO2/FiO2 <20kPa)
    • Bowel obstruction
    • Patient refusal
  • Pregnancy
  • Severe hepatic failure (ascites, hepatic encephalopathy or bilirubin >100umol/L)
  • Severe chronic cardiac failure (NYHA class III or IV)
  • Bleeding diathesis (INR>1.5, platelets <80,000) in the absence of anticoagulation therapy

Sites / Locations

  • Guy's and St Thomas' NHS Foundation Trust

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

NIV

ECCO2R

Arm Description

Standard application of NIV in hypercapnic respiratory failure as per usual standard of care

Addition of ECCO2R to NIV in AECOPD

Outcomes

Primary Outcome Measures

Time to cessation NIV
Time to cessation of NIV is defined as from NIV commencement to 6 hours without NIV.

Secondary Outcome Measures

Mortality
Time to event analysis
This is a composite endpoint to assess the ability to complete the required elements of the study from screening to commencement of ECCO2R in a clinically relevant timeframe
Health-related quality of life (HRQoL)
Cannulation-related outcomes
composite outcome of cannulation related complications
haemolysis related to the intervention
work of breathing
Time to cessation ECCO2R
Defined as from the commencement of ECCO2R to 6 hours following cessation of CO2 removal
Time to normalisation of pH
Hospital Length of stay
Intubation rate
Incidence of tracheostomy
length of ICU stay
Tolerance of therapy
subjective dyspnoea
nutrition
total caloric intake during interventional period
Mobilisation
mobilisation from bed during the study period
thrombotic complications
measurement of thrombotic complications in the patient related to the device
respiratory mechanics

Full Information

First Posted
March 9, 2014
Last Updated
August 4, 2021
Sponsor
Guy's and St Thomas' NHS Foundation Trust
Collaborators
Alung Technologies
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1. Study Identification

Unique Protocol Identification Number
NCT02086084
Brief Title
ECCO2R as an Adjunct to NIV in AECOPD
Official Title
Extra-corporeal CO2 Removal as an Adjunct to Non-Invasive Ventilation in Acute Severe Exacerbations of COPD
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Completed
Study Start Date
December 1, 2015 (Actual)
Primary Completion Date
December 31, 2020 (Actual)
Study Completion Date
December 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Guy's and St Thomas' NHS Foundation Trust
Collaborators
Alung Technologies

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Chronic obstructive pulmonary disease (COPD) is one of the UKs commonest chronic diseases and is responsible for a significant number of acute hospital admissions. COPD is characterised by progressive destruction in the elastic tissue within the lung, causing respiratory failure. The clinical course of COPD is characterised by recurrent acute exacerbations (AECOPD), causing considerable morbidity and mortality. Patients with moderate to severe acute exacerbations present with increased work of breathing and hypercapnia. The standard for respiratory support in this setting is non-invasive ventilation (NIV), a management strategy underpinned by a considerable evidence base. However despite NIV, up to 30% of patients with AECOPD will 'fail' and require intubation and mechanical ventilation. The mortality rate for patients requiring NIV is approximately 4%, if conversion to mechanical ventilation occurs the mortality is 29%. The last decade has seen an increasing interest in the provision of extracorporeal support for respiratory failure. The key element that has underpinned improving survival has been technological advancement. This has resulted in pumps causing less blood trauma and inflammatory response, better percutaneous cannulation techniques and coated circuits with reduced heparin requirements. Overall this has significantly reduced the complications associated with the provision of extracorporeal support. One variation of this technique (extra-corporeal CO2 removal ECCO2R) allows CO2 clearance from the blood. This approach has been the subject of a number of animal experiments and uncontrolled human case series demonstrating improved arterial CO2 and reduced work of breathing. Our own unpublished series demonstrates the same physiological changes. However to date the benefits of this approach have not been tested in a randomised controlled trial. The hypothesis is that the addition of ECCO2R to NIV will shorten the duration of NIV and reduce likelihood of intubation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease
Keywords
Acute Exacerbation Chronic Obstructive Pulmonary Disease, AECOPD, Non invasive ventilation, NIV, Extracorporeal carbon dioxide removal, ECCO2R

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
21 (Actual)

8. Arms, Groups, and Interventions

Arm Title
NIV
Arm Type
Active Comparator
Arm Description
Standard application of NIV in hypercapnic respiratory failure as per usual standard of care
Arm Title
ECCO2R
Arm Type
Experimental
Arm Description
Addition of ECCO2R to NIV in AECOPD
Intervention Type
Device
Intervention Name(s)
NIV
Intervention Description
Standard care
Intervention Type
Device
Intervention Name(s)
ECCO2R
Other Intervention Name(s)
Haemolung
Intervention Description
Application of ECCO2R in addition to NIV
Primary Outcome Measure Information:
Title
Time to cessation NIV
Description
Time to cessation of NIV is defined as from NIV commencement to 6 hours without NIV.
Time Frame
participants will be followed for the duration of ICU stay, an expected average of 4 days
Secondary Outcome Measure Information:
Title
Mortality
Time Frame
at 90 days
Title
Time to event analysis
Description
This is a composite endpoint to assess the ability to complete the required elements of the study from screening to commencement of ECCO2R in a clinically relevant timeframe
Time Frame
initial phase of study, an expected average of 3 hours
Title
Health-related quality of life (HRQoL)
Time Frame
90 days
Title
Cannulation-related outcomes
Description
composite outcome of cannulation related complications
Time Frame
participants will be followed for the duration of ICU stay, an expected average of 4 days
Title
haemolysis related to the intervention
Time Frame
participants will be followed for the duration of ICU stay, an expected average of 4 days
Title
work of breathing
Time Frame
participants will be followed for the duration of ICU stay, an expected average of 4 days
Title
Time to cessation ECCO2R
Description
Defined as from the commencement of ECCO2R to 6 hours following cessation of CO2 removal
Time Frame
participants will be followed for the duration of ICU stay, an expected average of 4 days
Title
Time to normalisation of pH
Time Frame
participants will be followed for the duration of ICU stay, an expected average of 4 days
Title
Hospital Length of stay
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 10 days
Title
Intubation rate
Time Frame
participants will be followed for the duration of ICU stay, an expected average of 4 days
Title
Incidence of tracheostomy
Time Frame
participants will be followed for the duration of ICU stay, an expected average of 4 days
Title
length of ICU stay
Time Frame
participants will be followed for the duration of ICU stay, an expected average of 4 days
Title
Tolerance of therapy
Time Frame
participants will be followed for the duration of ICU stay, an expected average of 4 days
Title
subjective dyspnoea
Time Frame
participants will be followed for the duration of ICU stay, an expected average of 4 days
Title
nutrition
Description
total caloric intake during interventional period
Time Frame
participants will be followed for the duration of ICU stay, an expected average of 4 days
Title
Mobilisation
Description
mobilisation from bed during the study period
Time Frame
participants will be followed for the duration of ICU stay, an expected average of 4 days
Title
thrombotic complications
Description
measurement of thrombotic complications in the patient related to the device
Time Frame
participants will be followed for the duration of ICU stay, an expected average of 4 days
Title
respiratory mechanics
Time Frame
participants will be followed for the duration of ICU stay, an expected average of 4 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria Known COPD with an acute exacerbation. An acute exacerbation is defined as per the GOLD criteria as an increase in dyspnoea, cough and/or sputum over the patient's normal symptoms. A severe exacerbation is defined as one requiring hospital admission. Patients with a persistent arterial pH<7.30 due primarily to hypercapnic respiratory failure after standard medical therapy and at least 1 hour of NIV. Age over 18 Exclusion Criteria Haemodynamic instability after ensuring euvolaemia Acute multiple organ failure requiring other organ supportive therapy, including indication for intubation and mechanical ventilation Known allergy/intolerance of heparin including known heparin induced thrombosis and thrombocytopaenia Acute uncontrolled haemorrhage Intracerebral haemorrhage Recent (<6 months) ischaemic cerebrovascular accident Organ transplant recipient Expected to die within 24 hours Venous abnormality or body habitus precluding cannulation Contraindication to NIV (as per British Thoracic Society recommendation) Facial burns/trauma/recent facial or upper airway surgery Vomiting Fixed upper airway obstruction Undrained pneumothorax Recent upper gastrointestinal surgery Inability to protect the airway Life threatening hypoxaemia (PaO2/FiO2 <20kPa) Bowel obstruction Patient refusal Pregnancy Severe hepatic failure (ascites, hepatic encephalopathy or bilirubin >100umol/L) Severe chronic cardiac failure (NYHA class III or IV) Bleeding diathesis (INR>1.5, platelets <80,000) in the absence of anticoagulation therapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nicholas Barrett, FCICM
Organizational Affiliation
Guy's and St Thomas' NHS Foundation Trust
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Luigi Camporota, PhD
Organizational Affiliation
Guy's and St Thomas' NHS Foundation Trust
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Nicholas Hart, PhD
Organizational Affiliation
Guy's and St Thomas' NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Guy's and St Thomas' NHS Foundation Trust
City
London
ZIP/Postal Code
SE1 7EH
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
35445986
Citation
Barrett NA, Hart N, Daly KJR, Marotti M, Kostakou E, Carlin C, Lua S, Singh S, Bentley A, Douiri A, Camporota L. A randomised controlled trial of non-invasive ventilation compared with extracorporeal carbon dioxide removal for acute hypercapnic exacerbations of chronic obstructive pulmonary disease. Ann Intensive Care. 2022 Apr 21;12(1):36. doi: 10.1186/s13613-022-01006-8.
Results Reference
derived
PubMed Identifier
31928313
Citation
Barrett NA, Hart N, Camporota L. In vivo carbon dioxide clearance of a low-flow extracorporeal carbon dioxide removal circuit in patients with acute exacerbations of chronic obstructive pulmonary disease. Perfusion. 2020 Jul;35(5):436-441. doi: 10.1177/0267659119896531. Epub 2020 Jan 11.
Results Reference
derived
PubMed Identifier
31362776
Citation
Barrett NA, Kostakou E, Hart N, Douiri A, Camporota L. Extracorporeal carbon dioxide removal for acute hypercapnic exacerbations of chronic obstructive pulmonary disease: study protocol for a randomised controlled trial. Trials. 2019 Jul 30;20(1):465. doi: 10.1186/s13063-019-3548-4.
Results Reference
derived

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ECCO2R as an Adjunct to NIV in AECOPD

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