HHV8 and Solid Organ Transplantation

Sponsor
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico (Other)
Overall Status
Recruiting
CT.gov ID
NCT05081141
Collaborator
(none)
250
1
51.5
4.9

Study Details

Study Description

Brief Summary

Solid organ transplant candidates will undergo serological screening for HHV8 at time of listing and transplantation.

In the event of a recipient/donor mismatch R-/D+ or in the presence of a seropositive recipient (R+), blood levels of HHV8 DNA will be monitored together with specific IGRA for HHV8.

Detailed Description

Patients on the waiting list for solid organ transplantation will undergo serological screening for HHV8 (lytic and latent antigens) in the pre-transplant phase, both at time of listing and then at the time of transplantation; if seropositivity is found, further investigations will be performed, i.e. blood levels of HHV8 DNA and specific Elispot for HHV8.

As for donors, serological testing for HHV8 (lytic and latent antigens) will be performed.

AFTER SOLID ORGAN TRANSPLANTATION

  • Patients found HHV8 seropositive in the pretransplant phase (R +), being at risk of HHV8 reactivation, will be monitored monthly in terms of viremia (HHV8 DNA) and specific IGRA for HHV8 for the first 6 months after transplantation and subsequently every 3 months up to 12 months post transplant.

  • In case of patients who were found HHV8 seronegative at time of transplantation, donor serology will be evaluated. In case of R-/D+ mismatch, SOT recipients will receive the same monitoring of R + patients (blood levels of HHV8 DNA and specific IGRA for HHV8 monthly for the first 6 months and then every 3 months up to 12 months after transplantation).

  • With reference to lung transplant patients, in cases of R + or R- / D +, HHV8 DNA will also be searched on the BAL obtained during surveillance bronchoscopies (usually at 3, 6 and 12 months after transplantation).

Study Design

Study Type:
Observational
Anticipated Enrollment :
250 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Screening for HHV8 Infection in Solid Organ Transplantation Donors, Candidates and Recipients
Actual Study Start Date :
Sep 15, 2021
Anticipated Primary Completion Date :
Dec 31, 2024
Anticipated Study Completion Date :
Dec 31, 2025

Arms and Interventions

Arm Intervention/Treatment
SOT Donors

Solid organ transplantation donors

Diagnostic Test: Diagnostic test for HHV8 exposure
Venipuncture for blood sampling

LuTx candidates and recipients

Lung transplant candidates and recipients

Diagnostic Test: Diagnostic test for HHV8 exposure
Venipuncture for blood sampling

LTx candidates and recipients

Liver transplant candidates and recipients

Diagnostic Test: Diagnostic test for HHV8 exposure
Venipuncture for blood sampling

KTx candidates and recipients

Kidney transplant candidates and recipients

Diagnostic Test: Diagnostic test for HHV8 exposure
Venipuncture for blood sampling

Outcome Measures

Primary Outcome Measures

  1. Incidence of HHV8 seropositivity among SOT donors and recipients [2021-2024]

    Incidence of HHV8 seropositivity among solid organ transplantations donors, candidates and recipients

  2. Incidence of HHV8 mismatch between SOT donors and recipients [2021-2024]

    Incidence of HHV8 mismatch between solid organ transplantations donors and recipients

Secondary Outcome Measures

  1. Incidence of HHV8 related disease after solid organ transplantation [2021-2025]

    Incidence of HHV8 related disease after solid organ transplantation

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
SOT DONORS:
Inclusion Criteria:
  • all donors used for transplantation purposes (kidney, liver, lung), including living donors in case of kidney transplantation
Exclusion Criteria:
  • None
SOT CANDIDATES RECIPIENTS:
Inclusion Criteria:
  • All patients listed for solid organ transplantation (lung, liver and kidney)
Exclusion Criteria:
  • None

Contacts and Locations

Locations

Site City State Country Postal Code
1 Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico di Milano Milan Italy 20122

Sponsors and Collaborators

  • Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
ClinicalTrials.gov Identifier:
NCT05081141
Other Study ID Numbers:
  • S_OTTO
First Posted:
Oct 18, 2021
Last Update Posted:
Oct 18, 2021
Last Verified:
Feb 1, 2021
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 Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 18, 2021