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Cardiopulmonary Stress Testing (CPET) AlloSure Study

Baylor Scott and White Health (BSWH) logo

Baylor Scott and White Health (BSWH)

Status

Enrolling

Conditions

Transplant; Failure, Heart
Heart Failure

Treatments

Behavioral: CPET exercise testing

Study type

Observational

Funder types

Other

Identifiers

NCT04656080
020-188

Details and patient eligibility

About

  1. Cell-free DNA does not vary significantly as a function of the activity of immunologically quiescent cardiac transplant recipients, despite the metabolic demands of the transplanted organ. (The implication of the null result would be that no restrictions to patient activity, nor modification of cardiac rehabilitation prescription, would be necessary to maintain proper test characteristics of AlloSure testing).
  2. In immunologically active cardiac transplant allografts, exercise prior to assay of donor-derived cell-free DNA can be used to increase the sensitivity of the AlloSure test. (The implication of this would be that the optimal time-frame for drawing an Allosure may actually be post-exercise, and that window will be characterized).

Full description

The specific research questioned aimed to be addressed with this proposed study are:

i. Are dd-cfDNA levels in heart transplant recipients independent of recent cardiopulmonary exercise? More specifically, does the metabolic demand of maximal cardiopulmonary exercise in recent heart transplant recipients trigger a release of dd-cfDNA (if so, then what is the time course for resolution back to baseline?) ii. If dd-cfDNA does not release to any significant degree with cardiac allografts with short donor-ischemic time, does this test characteristic continue to hold for cardiac allografts transplanted after longer donor ischemic times? iii. In cardiac transplant recipients with medically stabilized, treated antibody-mediated rejection (AMR) and persistent dd-cfDNA elevation, does a discrete episode of maximal cardiometabolic activity trigger any additional elevation of dd-cfDNA, and again, with what time course?

Enrollment

27 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Post-orthotopic heart transplant patients

Exclusion criteria

  1. orthopedic, neurologic and/or any other limitations that do not allow for exercise testing on a treadmill or cycle ergometer;
  2. individuals who require supplemental oxygen or have current permanent tracheostomies will be excluded from this study;
  3. individuals who are discharged to a long-term acute care facility;
  4. skilled nursing facility or with palliative care or hospice care will be excluded; (e) inmates and pregnant women;

(f) patients with antibody-mediate rejection that are not felt to be safe for cardiopulmonary stress testing.

Trial design

27 participants in 2 patient groups

transplant recipients <1year without AMR
Description:
20 recent transplant recipients (\<1 year) without antibody-mediated rejection (AMR);
Treatment:
Behavioral: CPET exercise testing
3 months post-heart transplant with AMR
Description:
• 7 transplant recipients, at least 3 months post-transplant, with antibody-mediated rejection
Treatment:
Behavioral: CPET exercise testing

Trial contacts and locations

1

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Central trial contact

Aayla Jamil, MBBS MPH

Data sourced from clinicaltrials.gov

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