NCAMR-CAMR Allosure Study

Sponsor
Tampa General Hospital (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT04217343
Collaborator
(none)
30
1
36
0.8

Study Details

Study Description

Brief Summary

Heart Transplant recipients at Tampa General Hospital heart transplant program who have pAMR1(H+) or pAMR1(I+) rejection will have a DD-cfDNA /GEP sample obtained at the time of the rejection. The DD-cfDNA/GEP will then be drawn every month post treatment for the rejection until the DD-cfDNA/GEP level returns to normal. A total of fifteen recipients with pAMR1(H+) and fifteen recipients with pAMR1(I+) rejection will be included in the study which will last two years. The presence of HLA antibodies (DSA's) and the titers, presence of Autoantibodies, the measurement of cytokines IL2, IL4, IL6, IL 10, IL 17, TNF alpha, TGF beta, the presence of coronary artery vasculopathy, the time from transplant to the onset of the episode of AMR, time to resolution, the response to treatment and comparison to the DD-cfDNA/GEP level with pAMR2 and pAMR 3 rejections will be analyzed.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Allosure/Allomap/Cytokines testing

Study Design

Study Type:
Observational
Anticipated Enrollment :
30 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
NON-COMPLEMENT MEDIATED AMR vs. COMPLEMENT MEDIATED AMR: DOES DD-cfDNA/GEP SHOW A DIFFERENCE
Actual Study Start Date :
Mar 5, 2020
Anticipated Primary Completion Date :
Mar 5, 2023
Anticipated Study Completion Date :
Mar 5, 2023

Arms and Interventions

Arm Intervention/Treatment
non-complement mediated pAMR(H+)

Diagnostic Test: Allosure/Allomap/Cytokines testing
All patients with evidence of Cardiac Transplant rejection will undergo Allosure, Allomap, and cytokine testing. Allosure and Allomap will be performed as part of routine care. Cytokine testing will be performed at time of rejection and resolution.

complement mediated pAMR(I+)

Diagnostic Test: Allosure/Allomap/Cytokines testing
All patients with evidence of Cardiac Transplant rejection will undergo Allosure, Allomap, and cytokine testing. Allosure and Allomap will be performed as part of routine care. Cytokine testing will be performed at time of rejection and resolution.

Outcome Measures

Primary Outcome Measures

  1. The level of dd-cfDNA in non-compliment mediated pAMR1 (H+) and complement mediated pAMR1 (I+) heart transplant rejection will be measured. [2 years]

    The level of dd-cfDNA in non-compliment mediated pAMR1 (H+) and complement mediated pAMR1 (I+) heart transplant rejection will be measured and then compared statistically to each other via Students t test as well as to the level of dd-cf DNA before and after the rejection episode.

Secondary Outcome Measures

  1. The level of inflammatory cytokines in non-compliment mediated pAMR1(H+) and compliment mediated pAMR1(I+) heart transplant rejection will be measured. [2 years]

    The level of inflammatory cytokines in non-compliment mediated pAMR1(H+) and compliment mediated pAMR1(I+) heart transplant rejection will be measured and compared statistically to each other via the Students t test as well as to the level of inflammatory cytokines after the rejection episode has resolved. The cytokines that will be assessed are: IL2, IL4, IL6, IL10, IL17, TNF alpha and TGF beta.

  2. The presence of HLA antibodies (DSA's) and titer levels, autoantibodies and titer levels and coronary artery vasculopathy will be measured. [2 years]

    The presence of HLA antibodies (DSA's) and titer levels, autoantibodies and titer levels and coronary artery vasculopathy will be measured in the heart transplant recipients with non-compliment mediated pAMR1(H+) and pAMR1(I+) rejection and compared to each other via Students t test.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 99 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients who have undergone Orthotopic Heart Transplantation who have pAMR1 rejection.
Exclusion Criteria:
  • Subjects less than 18 years old

Contacts and Locations

Locations

Site City State Country Postal Code
1 Tampa General Hospital Tampa Florida United States 33606

Sponsors and Collaborators

  • Tampa General Hospital

Investigators

  • Principal Investigator: Benjamin Mackie, MD, Tampa General Hospital/Tampa General Medical Group

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Benjamin Mackie, Principal Investigator/Medical Doctor, Tampa General Hospital
ClinicalTrials.gov Identifier:
NCT04217343
Other Study ID Numbers:
  • 19-0118
First Posted:
Jan 3, 2020
Last Update Posted:
Aug 22, 2022
Last Verified:
Aug 1, 2022
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 Benjamin Mackie, Principal Investigator/Medical Doctor, Tampa General Hospital

Study Results

No Results Posted as of Aug 22, 2022