DIASPORA: Diaphragm Structure and Pathobiology in Patients Being Bridged to Lung Transplant

Sponsor
University Health Network, Toronto (Other)
Overall Status
Recruiting
CT.gov ID
NCT03667027
Collaborator
The Hospital for Sick Children (Other)
40
1
45
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Study Details

Study Description

Brief Summary

This study is designed to characterize the changes in diaphragm structure, function and biology during bridging to lung transplant by mechanical ventilation or extracorporeal life support.

Condition or Disease Intervention/Treatment Phase
  • Device: Respiratory support

Detailed Description

Mechanical ventilation has been linked to diaphragm injury and dysfunction. During mechanical ventilation, the amount of breathing work done by the diaphragm is unpredictable: the diaphragm could be completely rested, or it could be overworked. Either of these possibilities may cause injury to the diaphragm. Patients with an injured and dysfunctional diaphragm have greater difficulty weaning from mechanical ventilation - they become too weak to breathe. However, little is known about the relationship between changes in the diaphragm and the histological (structure of cells and tissue) basis of these changes. The investigators have developed a new technique employing beside ultrasound to measure diaphragm thickness. This allows them to observe changes in diaphragm muscle structure and function.

The goal of the study is to determine whether different forms of respiratory support (mechanical ventilation vs extracorporeal life support) lead to different degrees of diaphragm injury and to compare changes in the diaphragm seen on ultrasound to changes in the diaphragm tissues under a microscope. This will help the investigators to confirm the best way to avoid diaphragm injury and to understanding the meaning of diaphragm ultrasound images.

Study Design

Study Type:
Observational
Anticipated Enrollment :
40 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Diaphragm Structure and Pathobiology in Patients Being Bridged to Lung Transplant
Actual Study Start Date :
Apr 1, 2019
Anticipated Primary Completion Date :
Oct 30, 2022
Anticipated Study Completion Date :
Dec 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Patients undergoing LTx with respiratory failure (cases)

Patients are receiving a respiratory support modality (mechanical ventilation and/or extracorporeal life support) as a bridge to lung transplantation (LTx).

Device: Respiratory support
Mechanical ventilation or extracorporeal life support

Patients undergoing LTx without prior respiratory support

Patients undergoing lung transplantation but do not require prior bridging respiratory support.

Elective thoracic surgical patients

Patients undergoing elective thoracic surgery for planned lung or esophageal resection.

Outcome Measures

Primary Outcome Measures

  1. Difference in diaphragm thickness and thickening fraction in patients using MV and patients using ECLS [Change from baseline diaphragm thickness and thickening fraction at 7 days after lung transplant]

    Diaphragm thickness and injury score will be tested for an interaction between the bridging modality (MV vs. ECLS) and the duration of exposure to the modality on the degree of diaphragm injury and atrophy

Secondary Outcome Measures

  1. Correlate changes in diaphragm thickness and histological features of diaphragm dysfunction [Assessed immediately after transplantation]

    Histological features to be assessed are: myofibril cross-sectional area, muscle fiber type, presence of cellular infiltrates, myofiber necrosis and regeneration, autophagy and fibro-fatty infiltration

  2. Biomarkers for diaphragm dysfunction [Assessed immediately before transplantation]

    Biomarkers to be assessed are: skeletal troponin-I and markers of systemic inflammation (IL-1, IL-6, Tumor Necrosis Factor (TNF)-alpha)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria (Cases):
  • Receiving a respiratory support modality as a bridge to lung transplantation

  • Formally listed for transplantation

Inclusion Criteria (Control Group 1):
  • Undergoing lung transplantation for either obstructive or restrictive lung disease
Inclusion Criteria (Control Group 2):
  • Undergoing elective thoracic surgery without any prior history of chronic pulmonary parenchymal disease
Exclusion Criteria (Cases and Controls):
  • Previously diagnosed with neuromuscular disorder

  • Received invasive mechanical ventilation for >48 hours in the preceding four weeks

  • Thoracic cage deformity

Contacts and Locations

Locations

Site City State Country Postal Code
1 Toronto General Hospital Toronto Canada

Sponsors and Collaborators

  • University Health Network, Toronto
  • The Hospital for Sick Children

Investigators

  • Principal Investigator: Ewan Goligher, MD, PhD, University Health Network, Toronto

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ewan Goligher, Intensivist, University Health Network, Toronto
ClinicalTrials.gov Identifier:
NCT03667027
Other Study ID Numbers:
  • 18-5660
First Posted:
Sep 12, 2018
Last Update Posted:
Nov 11, 2021
Last Verified:
Nov 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ewan Goligher, Intensivist, University Health Network, Toronto
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 11, 2021