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Goal of Open Lung Ventilation in Donors (GOLD)

Primary Purpose

Brain Death, Organ Donation, Organ Transplant Failure or Rejection

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Open lung protective ventilation
Conventional ventilation
Sponsored by
Vanderbilt University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Brain Death

Eligibility Criteria

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

Inclusion Criteria:

  • Brain death
  • Authorization for research
  • ≥13 years of age

Exclusion Criteria:

  • Arterial/Inspired oxygen ratio (PaO2/FiO2) ≤ 150 mmHg
  • PaO2/FiO2 ≥ 400 mmHg
  • BMI > 40
  • Hepatitis B surface antigen positive
  • Hepatitis C positive
  • Failure to complete donation process
  • Hemodynamic instability

Sites / Locations

  • UCLA
  • Stanford University
  • University of California San Francisco
  • Donor Network West

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Open Lung Protective Ventilation

Conventional Ventilation

Arm Description

Volume cycled assist control ventilation with tidal volume 8 cc/kg predicted body weight, PEEP 10 cm water (H2O), recruitment maneuvers every 8 hours and after any ventilator disconnect

Volume cycled assist control ventilation with tidal volume 10 cc/kg predicted body weight, PEEP 5 cm H2O, recruitment maneuvers after any ventilator disconnect

Outcomes

Primary Outcome Measures

Donor lung utilization rate
Percent of donor lungs procured and transplanted into recipient

Secondary Outcome Measures

Donor lung utilization in likely donors
Percent of donor lungs used from donors with < 50 pack year smoking, age < 65, negative serologies, and no underlying chronic lung disease
Donor oxygenation
Change in donor arterial oxygen (PaO2) from enrollment to procurement
Donor static compliance of the respiratory system
Change in compliance of the respiratory system (in ml/cm H2O) from enrollment to procurement. Static compliance (Cstat) is calculated as Cstat = ΔV / Pplat - PEEP where V is the volume delivered by the ventilator, Pplat is the end-inspiratory plateau pressure and PEEP is the level of positive end expiratory pressure.
Donor radiographic atelectasis scoring
Change in chest radiograph atelectasis score from enrollment to procurement
Recipient primary graft dysfunction
International Society of Heart and Lung Transplantation grade 2 or 3 primary graft dysfunction in lung transplant recipient
Recipient mortality
Lung transplant recipient death

Full Information

First Posted
February 14, 2018
Last Updated
May 3, 2021
Sponsor
Vanderbilt University Medical Center
Collaborators
University of California, San Francisco, University of California, Los Angeles, Stanford University, Donor Network West
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1. Study Identification

Unique Protocol Identification Number
NCT03439995
Brief Title
Goal of Open Lung Ventilation in Donors
Acronym
GOLD
Official Title
Goal of Open Lung Ventilation in Donors
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Terminated
Why Stopped
Trial no longer feasible
Study Start Date
July 9, 2018 (Actual)
Primary Completion Date
January 1, 2020 (Actual)
Study Completion Date
January 1, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Vanderbilt University Medical Center
Collaborators
University of California, San Francisco, University of California, Los Angeles, Stanford University, Donor Network West

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The primary goal of this study is to assess whether ventilation of deceased organ donors with an open lung protective ventilatory strategy will improve donor lung utilization rates and donor oxygenation compared to a conventional ventilatory strategy.
Detailed Description
Deceased organ donors are maintained on life support including mechanical ventilation during the time between brain death and organ procurement. The optimal mode of mechanical ventilation for deceased organ donors has not been definitively established. Since deceased organ donors may develop atelectasis leading to impaired oxygenation, an open lung protective ventilatory strategy with higher positive end expiratory pressure (PEEP), lower tidal volume and recruitment maneuvers has been hypothesized to be beneficial. Favorable outcomes were observed in a European clinical trial comparing open lung protective ventilation (OLPV) to a conventional ventilatory strategy in terms of donor oxygenation and lung utilization for transplantation (Mascia L et al, Journal of the American Medical Association 2010). However, donor management procedures in Europe are much shorter in duration compared to the US and it is not clear that these findings are generalizable to the US donor management environment. The GOLD trial will test the effect of an OLPV strategy compared to conventional ventilation (CV) in the US donor management environment. This multi center trial will enroll 400 brain dead organ donors randomized into 1 of 2 treatment arms. After randomization, mechanical ventilation will be protocolized according to treatment arm with one arm receiving control ventilation (CV) utilizing standard Donor Network West (DNW) protocols and the other arm receiving the OLPV strategy with higher positive end expiratory pressure (PEEP) and lower tidal volume compared to CV. The primary outcomes is donor lung utilization for transplantation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Death, Organ Donation, Organ Transplant Failure or Rejection

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Enrolled donors will be randomly assigned to two different modes of mechanical ventilation for the duration of donor management
Masking
Outcomes Assessor
Masking Description
Outcomes in donors and lung transplant recipients will be done by assessors who are blinded to ventilator treatment assignment
Allocation
Randomized
Enrollment
154 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Open Lung Protective Ventilation
Arm Type
Experimental
Arm Description
Volume cycled assist control ventilation with tidal volume 8 cc/kg predicted body weight, PEEP 10 cm water (H2O), recruitment maneuvers every 8 hours and after any ventilator disconnect
Arm Title
Conventional Ventilation
Arm Type
Active Comparator
Arm Description
Volume cycled assist control ventilation with tidal volume 10 cc/kg predicted body weight, PEEP 5 cm H2O, recruitment maneuvers after any ventilator disconnect
Intervention Type
Other
Intervention Name(s)
Open lung protective ventilation
Intervention Description
Higher PEEP, lower tidal volume mechanical ventilation
Intervention Type
Other
Intervention Name(s)
Conventional ventilation
Intervention Description
Lower PEEP, standard tidal volume mechanical ventilation
Primary Outcome Measure Information:
Title
Donor lung utilization rate
Description
Percent of donor lungs procured and transplanted into recipient
Time Frame
during donor management period (usually 12-48 hours)
Secondary Outcome Measure Information:
Title
Donor lung utilization in likely donors
Description
Percent of donor lungs used from donors with < 50 pack year smoking, age < 65, negative serologies, and no underlying chronic lung disease
Time Frame
during donor management period (usually 12-48 hours)
Title
Donor oxygenation
Description
Change in donor arterial oxygen (PaO2) from enrollment to procurement
Time Frame
during donor management period (usually 12-48 hours)
Title
Donor static compliance of the respiratory system
Description
Change in compliance of the respiratory system (in ml/cm H2O) from enrollment to procurement. Static compliance (Cstat) is calculated as Cstat = ΔV / Pplat - PEEP where V is the volume delivered by the ventilator, Pplat is the end-inspiratory plateau pressure and PEEP is the level of positive end expiratory pressure.
Time Frame
during donor management period (usually 12-48 hours)
Title
Donor radiographic atelectasis scoring
Description
Change in chest radiograph atelectasis score from enrollment to procurement
Time Frame
during donor management period (usually 12-48 hours)
Title
Recipient primary graft dysfunction
Description
International Society of Heart and Lung Transplantation grade 2 or 3 primary graft dysfunction in lung transplant recipient
Time Frame
72 hours after transplant
Title
Recipient mortality
Description
Lung transplant recipient death
Time Frame
30 days after transplant

10. Eligibility

Sex
All
Minimum Age & Unit of Time
13 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Brain death Authorization for research ≥13 years of age Exclusion Criteria: Arterial/Inspired oxygen ratio (PaO2/FiO2) ≤ 150 mmHg PaO2/FiO2 ≥ 400 mmHg BMI > 40 Hepatitis B surface antigen positive Hepatitis C positive Failure to complete donation process Hemodynamic instability
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lorraine B Ware, MD
Organizational Affiliation
Vanderbilt University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
UCLA
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095
Country
United States
Facility Name
Stanford University
City
Palo Alto
State/Province
California
ZIP/Postal Code
94305
Country
United States
Facility Name
University of California San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States
Facility Name
Donor Network West
City
San Ramon
State/Province
California
ZIP/Postal Code
94583
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
21156950
Citation
Mascia L, Pasero D, Slutsky AS, Arguis MJ, Berardino M, Grasso S, Munari M, Boifava S, Cornara G, Della Corte F, Vivaldi N, Malacarne P, Del Gaudio P, Livigni S, Zavala E, Filippini C, Martin EL, Donadio PP, Mastromauro I, Ranieri VM. Effect of a lung protective strategy for organ donors on eligibility and availability of lungs for transplantation: a randomized controlled trial. JAMA. 2010 Dec 15;304(23):2620-7. doi: 10.1001/jama.2010.1796.
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Goal of Open Lung Ventilation in Donors

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