Study Stopped
loss of funding
Endothelial Injury and Development of Coronary Intimal Thickening After Heart Transplantation
2 other identifiers
interventional
12
1 country
1
Brief Summary
Coronary allograft vasculopathy (CAV) is the leading cause of late graft failure and second leading cause of late mortality after heart transplantation. CAV has been associated with a variety of traditional risk factors for atherosclerosis; however, immune mediated injury from development of de-novo donor-specific antibodies after transplantation also likely plays an important role. Similar to the progression of traditional atherosclerosis, it is likely that endothelial dysfunction is the precursor to the development of intimal thickening and CAV. The investigators hypothesize that coronary allograft vasculopathy after heart transplantation as defined by progressive neointimal hyperplasia is preceded by endothelial dysfunction, which in turn is at least partly mediated by donor specific antibodies. The investigators are proposing a prospective study in humans to test the above hypothesis and further mechanistically understand how CAV progresses. In this study the investigators will test for coronary endothelial function by infusing acetylcholine into the coronary artery and measure intimal hyperplasia by optical coherence tomography (OCT) and compare findings in patients with and without donor specific antibodies.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_1
Started Sep 2012
Longer than P75 for phase_1
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2012
CompletedFirst Submitted
Initial submission to the registry
May 2, 2013
CompletedFirst Posted
Study publicly available on registry
May 7, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2017
CompletedSeptember 6, 2017
September 1, 2017
2 years
May 2, 2013
September 1, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
The primary endpoint will be a comparison of intimal thickness in the coronary artery by Optical Coherence Tomography with presence or absence of donor specific antibodies.
baseline (year 1 post transplant) and annually for 2 years
Secondary Outcomes (6)
Assessment of epicardial coronary endothelial function by measuring change in vessel size in response to acetylcholine and how this compares to peripheral endothelial function.
baseline (year 1 post transplant) and annually for 2 years
Prospectively determine the association of HLA and non-HLA donor specific antibodies that activate complement with endothelial dysfunction and intimal thickening.
baseline (year 1 post transplant) and annually for 2 years
Gene expression of white blood cells by microRNA and how this relates to endothelial function and intimal thickness.
baseline (year 1 post transplant) and annually for 2 years
Plaque characterization in coronary artery by OCT
baseline (year 1 post transplant) and annually for 2 years
Natural progression of coronary allograft vasculopathy over first 2 years after transplantation
baseline (year 1 post transplant) and annually for 2 years
- +1 more secondary outcomes
Study Arms (1)
Single arm
EXPERIMENTALAll subjects will undergo a Brachial Artery Flow Medicated Dilation prior to heart catheterization. After routine heart catheterization, images of their coronary artery will be recorded by Optical Coherence Tomography (OCT) during infusion of Acetylcholine.
Interventions
OCT imaging of the LAD coronary artery
Infusion in the coronary artery to study endothelial function
Assess peripheral brachial artery endothelial function
Eligibility Criteria
You may qualify if:
- Subjects who are 1 year post heart transplantation
- Subjects will include both male and females
- Be at least 18 years of age
You may not qualify if:
- Known coronary artery disease after transplantation
- Evidence of strong or moderate antibodies already present at the time of the transplant
- Severe renal dysfunction defined as creatinine clearance of \<30 or on hemodialysis.
- or more episodes of acute cellular rejection
- Females who are pregnant
- Patients requiring endomyocardial biopsy at the time of catheterization
- Patients unable to tolerate heparin or systemic anticoagulation
- History of multi-organ transplant
- Patients unable to give consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Pittsburgh Medical Center
Pittsburgh, Pennsylvania, 15213, United States
Related Publications (1)
Khandhar SJ, Yamamoto H, Teuteberg JJ, Shullo MA, Bezerra HG, Costa MA, Selzer F, Lee JS, Marroquin OC, McNamara DM, Mulukutla SR, Toma C. Optical coherence tomography for characterization of cardiac allograft vasculopathy after heart transplantation (OCTCAV study). J Heart Lung Transplant. 2013 Jun;32(6):596-602. doi: 10.1016/j.healun.2013.02.005. Epub 2013 Mar 15.
PMID: 23499356BACKGROUND
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Catalin Toma, MD
University of Pittsburgh
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- NA
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- INDIV
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
May 2, 2013
First Posted
May 7, 2013
Study Start
September 1, 2012
Primary Completion
September 1, 2014
Study Completion
May 1, 2017
Last Updated
September 6, 2017
Record last verified: 2017-09