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Stratified vs Routine Prophylaxis in Living Kidney Transplantation From HBsAg+ Donors to HBsAg- Recipients

S

Sichuan University

Status

Enrolling

Conditions

Kidney Transplantation
HBV

Treatments

Other: prophylaxis regimen

Study type

Observational

Funder types

Other

Identifiers

NCT04562051
WestChina-KT

Details and patient eligibility

About

This is a multicenter, prospective, observational study to compare the efficacy and safety of stratified prophylaxis based on donors' and recipients' risk factors vs routine prophylaxis bases on clinical experience in living kidney transplantation from HBsAg+ donors to HBsAg- recipients. The follow-up period was 2 years after renal transplantation. The primary outcome was prevention failure of HBV transmission (any one of HBsAg - → +, HBV DNA - → +, HBeAg - → +, HBeAb - → +, HBcAb - → +, active liver function damage and death in the recipient).

Enrollment

100 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. patients diagnosed with end-stage renal diseases and suitable for living kidney transplantation;
  2. HBsAg+ donor was the only donor;
  3. age and sex of donors and recipients were unrestricted;
  4. ABO compatible or incompatible between the donor and recipient;
  5. The living donor voluntarily donates one of their kidneys to the recipient free of charge;
  6. The donor and recipient can understand the purpose and risk of living KT and sign informed consent;
  7. Ethics committee approved.

Exclusion criteria

  1. preoperative abnormal liver dysfunction in the donor or recipient (ALT > 60IU/L for females, and >75 IU/L for males; or total bilirubin > 34 umol/L); or preoperative ultrasonography in the donor or recipient reported hepatic cirrhosis;
  2. positive complement-dependent cytotoxicity cross-match test;
  3. combined HCV or HIV infection in the donor or recipient;
  4. diagnosed with malignancy or had a history of malignancy in the past 5 years;
  5. non-kidney transplantation history.

Trial design

100 participants in 2 patient groups

stratified prophylaxis group
Description:
The process of stratified prophylaxis was as follows. 1) If the recipient's HBsAb level is more than 100 IU/L and the donor is HBV DNA-, the recipient will not receive any preventive measures; 2) If the recipient's HBsAb is more than 100 IU/L and the donor is HBV DNA+, the recipient receives antiviral treatment for 1 month; 3) If the recipient's HBsAb is between 10 and 100 IU/L, the recipient is treated with single dose HBIG and antiviral treatment for 1 month regardless of the donor's HBV DNA status; 4) If the recipient's HBsAb is less than 10 IU/L, the recipient will receive single dose HBIG and antiviral treatment for 1 month regardless of the donor's HBV DNA status.
Treatment:
Other: prophylaxis regimen
Routine prophylaxis group
Description:
Transplant centers adopted routine prophylaxis based on clinical experience
Treatment:
Other: prophylaxis regimen

Trial contacts and locations

1

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Central trial contact

Tao Lin, PhD

Data sourced from clinicaltrials.gov

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