Skip to content

Treating Donors With Intravenous Immunoglobulin to Reduce Donor-Derived Infections

Treating Donors With Intravenous Immunoglobulin to Reduce Donor-Derived Infections

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05799716
Enrollment
40
Registered
2023-04-05
Start date
2023-04-01
Completion date
2024-09-01
Last updated
2023-04-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Rejection of Renal Transplant, Bacteremia, Viremia

Keywords

IVIG Infection

Brief summary

The goal of this clinical trial is to learn about the benefit of IVIG in donor-derived infections and the potential immunomodulatory effect on transplanted organs. The main questions it aims to answer are: 1. How effective IVIG is in preventing donor-derived infections 2. Does IVIG has potential immunomodulatory effect on transplanted organs

Detailed description

Donor-derived infections are defined as any infection present in the donor that is transmitted to one or more recipient. Donor-derived infections can be categorized into two groups: expected and unexpected infections. Expected transmissions occur when the donor is known to have an infection, as demonstrated by positive serology or nucleic acid test (NAT) result for cytomegalovirus (CMV), Epstein-Barr virus (EBV) or hepatitis B and C, or positive cultures in the donor at the time of donation. Unexpected transmissions may occur despite current screening strategies and are not expected in the donor at the time of organ placement. Intravenous immunoglobulins (IVIG) are produced by pooling together of serum immunoglobulins from multiple donors, and are known to have powerful immunomodulatory and anti-inflammatory functions in vitro and in vivo. The goal of this study is to figure out the benefit of IVIG in donor-derived infections and the potential immunomodulatory effect on transplanted organs.

Interventions

DRUGIVIG

0.5g/Kg

Sponsors

Shanghai Changzheng Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
6 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Any person approved as a transplant donor with recipient who has never undergone a previous transplantation * Transplant donor must be 6 years old or older * They must have provided signed informed consent * The donors must be willing to contribute samples of blood

Exclusion criteria

* Any potential transplant donor who is receiving or have received anti-herpes medication in the past week * Any potential transplant donor to a recipient who has received a previous solid organ transplant * Any potential transplant donor who is immunosuppressed due to medical disease and/or immunosuppressive or immunomodulating medications * Any potential transplant donor who is on corticosteroids

Design outcomes

Primary

MeasureTime frameDescription
Next-Generation Sequencing (NGS) Results of Bacteremia or Viremia in Transplant Recipient14 daysNGS is a technology for determining the sequence of DNA or RNA to study genetic variation associated with diseases like bacteremia and viremia.
Incidence of Bacteremia or Viremia in Transplant Recipient14 days

Secondary

MeasureTime frame
Incidence of Acute Rejection in Transplant Recipient1 month

Contacts

Primary ContactJinghui Yang
yjh@smmu.edu.cn021-81885756

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026