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HIVNCT03170414

Observational Study of Solid Organ Transplantation Utilizing HIV-Positive Donors in HIV-Positive Recipients

An observational study of HIV and Awaiting Organ Transplant, run by University of Minnesota at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The primary objective of this study is to evaluate the safety of solid organ transplantation using HIV-positive deceased donors (liver, kidney) and HIV-positive living donors (liver) in HIV-positive recipients. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
HIV, Awaiting Organ Transplant
How many people
10 participants
Where
1 siteUnited States
Study dates
15 Jun 2017to 1 Dec 2023
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Adult, Older adult

Study population: Stable HIV-infected adults in need of a solid organ transplant (kidney, liver) who meet standard and study specified HIV criteria for organ transplantation will be offered enrollment in the study. Deceased donors (kidney, liver) and living donors (liver) will be utilized in this protocol. No living kidney donors will be enrolled.

RECIPIENT ELIGIBILITY CRITERIA HIV-Positive Recipient Inclusion Criteria (liver, kidney)

  1. Participant is able to understand and provide informed consent.
  2. Participant meets standard listing criteria for transplant.
  3. Documented HIV infection (by any licensed ELISA and confirmation by Western Blot, positive HIV ab IFA, or documented history of detectable HIV-1 RNA).
  4. Participant is ≥ 18 years old.
  5. No evidence of active opportunistic complications of HIV infection.
  6. Participant CD4+ T-cell count is >/= 200/µL within 16 weeks prior to transplant for kidney transplant recipients. For liver transplant recipient, CD4+ T-cell counts need to be >/= 100/ul (or >/= 200/µL if history of opportunistic infection) within 16 weeks prior to transplant.
  7. Participant most recent HIV-1 RNA < 50 copies/mL (by any FDA-approved assay performed in CLIA-approved laboratory), in the 26 weeks prior to transplant. Participants unable to tolerate ART due to organ failure or who have only recently started ART may have detectable viral load and still be considered eligible if the study team is confident there will be a safe, tolerable, and effective antiretroviral regimen once organ function is restored after transplantation.
  8. Concurrence by the study team that based on medical history and ART, viral suppression can be achieved in the recipient post-transplant.
  9. No history of primary CNS lymphoma or progressive PML.
  10. On a stable antiretroviral regimen. Participants unable to tolerate ART due to organ failure may still be considered eligible if the study team is confident there will be a safe, tolerable, and effective antiretroviral regimen once organ function is restored after transplantation.

HIV-Positive Recipient Exclusion Criteria (liver, kidney)

  1. Participant has concomitant conditions that, in the judgment of the investigators, would preclude transplantation or immunosuppression.

DONOR ELIGIBILITY CRITERIA HIV-Positive Deceased Donor (liver, kidney)

  1. Must meet all clinical criteria for HIV-uninfected organ donors.
  2. No evidence of invasive opportunistic complications of HIV infection.
  3. Pre-implant donor organ biopsy showing no disease process that would put the recipient at increased risk of rapid progression to end-stage organ failure, to be stored for the duration of the study.
  4. Donor has documented HIV infection (by any licensed ELISA and confirmation by Western Blot, positive HIV ab IFA, or history of detectable HIV-1 RNA) from a CLIA-approved laboratory.
  5. If known history of HIV infection and prior antiretroviral therapy, the study team must describe the anticipated post-transplant antiretroviral regimen to be prescribed for the recipient and justify its conclusion that the regimen will be safe, tolerable and effective.

HIV-Positive Living Donor (liver)

  1. Donor meets all clinical criteria to be a living liver donor other than being HIV positive.
  2. Donor has documented HIV infection (by any licensed ELISA and confirmation by Western Blot, positive HIV ab IFA, or history of detectable HIV-1 RNA) from a CLIA-approved laboratory.
  3. No evidence of invasive opportunistic complications of HIV infection
  4. Donor CD4+ T-cell count is >/= 500/µL in the 26 weeks prior to donation.
  5. The most recent HIV-1 RNA has been below 50 copies RNA/ml in the 26 weeks prior to donation.
  6. On a stable antiretroviral regimen.
  7. Must be evaluated by the HIV/Transplant Infectious Diseases team to verify resistance history and current ART regimens. The potential for transmission of resistant strain of HIV will be assessed.
  8. Pre-implant donor liver biopsy to be stored for the duration of the study showing no evidence of a disease process that would put the donor at increased risk of progressing to end-stage organ failure after donation, or that would present a risk of poor graft function to the recipient.
  9. Must be evaluated by an independent HIV study living donor advocate separate from the transplant service in addition to the living donor advocate seen by all living donors.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • University of Minnesota Medical Center

    Minneapolis, Minnesota, 55454

Other trials in United States

About this study

Official title: A Prospective Observational Study of Solid Organ Transplantation Utilizing HIV-Positive Donors in HIV-Positive Recipients

The primary objective of this study is to evaluate the safety of solid organ transplantation using HIV-positive deceased donors (liver, kidney) and HIV-positive living donors (liver) in HIV-positive recipients.

HIV-positive individuals who agree to accept and receive a solid organ transplant from and HIV-positive donor will be followed to determine the safety and efficacy of this practice.

Read the detailed description

This is a prospective observational study of solid organ transplantation utilizing HIV-positive donors in HIV-positive recipients. Stable HIV-infected adults in need of a solid organ transplant (kidney, liver) who meet standard and study specified HIV criteria for organ transplantation will be offered enrollment in the study. Deceased donors (kidney, liver) and living donors (liver) will be utilized in this protocol. No living kidney donors will be enrolled.

This study will evaluate overall survival and graft survival. In addition the study will assess potential complications of organ transplant using HIV+ donor organs, including but not limited to: HIV disease progression, development of antiretroviral resistance mutations, incidence of opportunistic infections, incidence of transplant complications, impacts of liver regeneration, incidence of viral-related malignancies, and incidence of HIV-superinfection.

Keywords
HIV, Kidney Transplant, Liver Transplant, Transplant, HOPE Act

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT03170414
Study groupRoleWhat they receive
HIV D+/R+HIV+ recipients who receive an organ transplant from an HIV+ donor

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Patient Survival

    Patient survival at one year.

    Measured: One Year

Secondary outcomes (11)
  1. Graft Survival

    Measured: Months 3, 6, 9, Years 1, 2, 3

  2. Incidence and Severity of Graft Rejection

    Measured: Through study completion, up to three years

  3. HIV Disease Progression

    Measured: Through study completion, up to three years

  4. Development of antiretroviral resistance mutations and/or X4 tropic virus in blood and allograft

    Measured: Through study completion, up to three years

  5. Incidence of bacterial, fungal, viral and other opportunistic infections

    Measured: Through study completion, up to three years

  6. Incidence of other transplant complications (surgical and vascular)

    Measured: Through study completion, up to three years

  7. Liver transplant recipients: Impact on liver regeneration

    Measured: Through study completion, up to three years

  8. Analysis of recurrent HIV associated nephropathy among kidney transplant recipients

    Measured: Through study completion, up to three years

  9. Incidence of other viral-related malignancies (HPV, EBV, HBV, HCV)

    Measured: Through study completion, up to three years

  10. Incidence of systemic HIV-superinfection in blood

    Measured: Through study completion, up to three years

  11. Incidence of tissue specific HIV-superinfection

    Measured: Through study completion, up to three years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted31 May 2017
  2. Study start15 Jun 2017
  3. Primary completion1 Dec 2023
  4. Study completion1 Dec 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
10 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03170414
Sponsor's protocol ID
SURG-2017-24985
Status last verified
Feb 2024
First submitted
23 May 2017
Last updated
12 Feb 2024
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of HIV and Awaiting Organ Transplant, run by University of Minnesota at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 12 Feb 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Patient Survival (time frame: One Year). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Feb 2024.

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