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.
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)
- Participant is able to understand and provide informed consent.
- Participant meets standard listing criteria for transplant.
- Documented HIV infection (by any licensed ELISA and confirmation by Western Blot, positive HIV ab IFA, or documented history of detectable HIV-1 RNA).
- Participant is ≥ 18 years old.
- No evidence of active opportunistic complications of HIV infection.
- 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.
- 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.
- Concurrence by the study team that based on medical history and ART, viral suppression can be achieved in the recipient post-transplant.
- No history of primary CNS lymphoma or progressive PML.
- 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)
- 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)
- Must meet all clinical criteria for HIV-uninfected organ donors.
- No evidence of invasive opportunistic complications of HIV infection.
- 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.
- 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.
- 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)
- Donor meets all clinical criteria to be a living liver donor other than being HIV positive.
- 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.
- No evidence of invasive opportunistic complications of HIV infection
- Donor CD4+ T-cell count is >/= 500/µL in the 26 weeks prior to donation.
- The most recent HIV-1 RNA has been below 50 copies RNA/ml in the 26 weeks prior to donation.
- On a stable antiretroviral regimen.
- 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.
- 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.
- 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
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.
- Conditions
- HIV, Awaiting Organ Transplant
- 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 group | Role | What 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.
Patient Survival
Patient survival at one year.
Measured: One Year
Secondary outcomes (11)
Graft Survival
Measured: Months 3, 6, 9, Years 1, 2, 3
Incidence and Severity of Graft Rejection
Measured: Through study completion, up to three years
HIV Disease Progression
Measured: Through study completion, up to three years
Development of antiretroviral resistance mutations and/or X4 tropic virus in blood and allograft
Measured: Through study completion, up to three years
Incidence of bacterial, fungal, viral and other opportunistic infections
Measured: Through study completion, up to three years
Incidence of other transplant complications (surgical and vascular)
Measured: Through study completion, up to three years
Liver transplant recipients: Impact on liver regeneration
Measured: Through study completion, up to three years
Analysis of recurrent HIV associated nephropathy among kidney transplant recipients
Measured: Through study completion, up to three years
Incidence of other viral-related malignancies (HPV, EBV, HBV, HCV)
Measured: Through study completion, up to three years
Incidence of systemic HIV-superinfection in blood
Measured: Through study completion, up to three years
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.
- First posted31 May 2017
- Study start15 Jun 2017
- Primary completion1 Dec 2023
- Study completion1 Dec 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for HIVStudies of the same condition, open and under way.
- More trials run by University of MinnesotaThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- University of Minnesota
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Timothy Pruett, MD, Principal investigator, University of Minnesota
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
Study at a glance
From the registry record, last updated by the sponsor on 12 Feb 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Prospective Observational Study of Solid Organ Transplantation Utilizing HIV-Positive Donors in HIV-Positive Recipients
- ClinicalTrials.gov ID
- NCT03170414
- Acronym / sponsor ID
- SURG-2017-24985
- Conditions
- HIV, Awaiting Organ Transplant
- Keywords
- HIV, Kidney Transplant, Liver Transplant, Transplant, HOPE Act
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 10 participants (actual)
- Lead sponsor
- University of MinnesotaUniversity, hospital or other
- Study start
- 15 Jun 2017 (actual)
- Primary completion
- 1 Dec 2023 (actual)
- Study completion
- 1 Dec 2023 (actual)
- First posted
- 31 May 2017 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| HIV D+/R+ | – | –HIV+ recipients who receive an organ transplant from an HIV+ donor |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Age groups
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Patient Survival
Time frame: One Year
Patient survival at one year.
11 secondary outcomes
Graft Survival
Time frame: Months 3, 6, 9, Years 1, 2, 3
Incidence and Severity of Graft Rejection
Time frame: Through study completion, up to three years
HIV Disease Progression
Time frame: Through study completion, up to three years
Development of antiretroviral resistance mutations and/or X4 tropic virus in blood and allograft
Time frame: Through study completion, up to three years
Incidence of bacterial, fungal, viral and other opportunistic infections
Time frame: Through study completion, up to three years
Incidence of other transplant complications (surgical and vascular)
Time frame: Through study completion, up to three years
Liver transplant recipients: Impact on liver regeneration
Time frame: Through study completion, up to three years
Analysis of recurrent HIV associated nephropathy among kidney transplant recipients
Time frame: Through study completion, up to three years
Incidence of other viral-related malignancies (HPV, EBV, HBV, HCV)
Time frame: Through study completion, up to three years
Incidence of systemic HIV-superinfection in blood
Time frame: Through study completion, up to three years
Incidence of tissue specific HIV-superinfection
Time frame: Through study completion, up to three years
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 Feb 2024.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Timothy Pruett, MD principal investigator
University of Minnesota
1 site in 1 country: see every site and its status.
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.