Assessing the Effects of Mechanical Unloading on Repair Version-1

NCT ID: NCT06026215

Last Updated: 2023-09-07

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 23 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2015-01-15
• Study Completion Date: 2019-05-31

Brief Summary

The mechanism by which heart failure initiates and progresses and the mechanisms of heart repair remain unclear.

The left ventricular assist device (LVAD) is a therapy to stabilise patients while they await their transplant. The LVAD helps pump blood around the body, giving the heart an opportunity to recover. During surgery, the apical core tissue is routinely removed to allow the implantation of the device (this tissue is normally discarded). Some patients demonstrate cardiac recovery, allowing the device to be removed without later needing a transplant. As part of the LVAD removal procedure, the section around the device might need to be removed (this tissue is normally discarded). To further understand the cellular and molecular mechanisms by which the heart is repaired, the investigators wish to utilise this surplus tissue for research purposes. The collection of this tissue is part of routine treatment and does not represent additional risk for the patient for research purposes. Some patients might still require a transplant following VAD treatment. The native heart is removed from these patients (routinely discarded) and replaced by a donor heart. The investigators wish to utilise this discarded tissue for research purposes, so that the investigators can identify the cellular and molecular factors involved in cardiac repair and which distinguish responsive and non-responsive patients. Heart transplant recipients who require extracorporeal membrane oxygenation will have an additional heart biopsy sample taken for research purposes when performed as part of routine clinical practice. There is no additional risk to the patient for research purposes. Heart failure patients scheduled for transplantation (who have not received a VAD) will be recruited prior to transplantation and their native heart retained for research purposes. An additional peripheral blood sample will be collected from all patients for research purposes when performed for routine clinical practice.

Conditions

Heart Failure; Transplant; Failure, Heart

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Group 1

Heart failure patients requiring ventricular assist device implantation will be included into group 1.

No interventions assigned to this group

Group 2

Heart transplant recipients requiring early extracorporeal membrane oxygenation will be recruited into group 2.

No interventions assigned to this group

Group 3

Heart transplant recipients who have not previously received a VAD will be recruited into group 3.

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• Patients must be able to provide informed consent; informed consent may be provided retrospectively if this cannot be provided pre-surgery.
• Patients must be aged between 18--70 years of age.
• Patients who have been clinically diagnosed with chronic heart failure and require mechanical unloading using a left ventricular assist device.
• Patients who have received a heart transplant but require extracorporeal membrane oxygenation.

Exclusion Criteria

• Patients under 18 or over 70 years of age.
• Patients unable to provide informed consent.
• Patients who are prisoners.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Manchester University NHS Foundation Trust

OTHER_GOV

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Other Identifiers

139009

Identifier Type: OTHER

Identifier Source: secondary_id

2015CD001

Identifier Type: -

Identifier Source: org_study_id