PINK: Pediatric Induction Therapy in Kidney Transplantation

Sponsor
Gang Chen (Other)
Overall Status
Completed
CT.gov ID
NCT06087003
Collaborator
Zhejiang University (Other), First Affiliated Hospital, Sun Yat-Sen University (Other), The First Affiliated Hospital of Zhengzhou University (Other), Changhai Hospital (Other)
958
5
126.9
191.6
1.5

Study Details

Study Description

Brief Summary

The goal of this observational study is to compare the efficacy of two most commonly used induction therapy for the prevention of acute rejection (AR) after renal transplantation in children. The main question it aims to answer is:

Is basiliximab (anti-CD25 monoclonal antibody) induction therapy effective and safe in preventing AR after kidney transplantation in children compared with anti-thymoglobulin polyclonal antibodies induction therapy?

The transplant and follow-up data of participants will be retrospectively collected.

Researchers will compare the rate of AR to see if basiliximab (anti-CD25 monoclonal antibody) induction therapy is a better option for certain pediatric kidney transplant recipients.

Condition or Disease Intervention/Treatment Phase
  • Drug: Basiliximab Injection
  • Drug: rabbit ATG

Study Design

Study Type:
Observational
Actual Enrollment :
958 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Induction Therapy of Thymoglobulin Versus Basiliximab in the Prevention of Acute Rejection After Pediatric Kidney Transplantation
Actual Study Start Date :
Mar 3, 2013
Actual Primary Completion Date :
Jul 27, 2022
Actual Study Completion Date :
Sep 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Basilliximab induction group

Basiliximab was administered intravenously 4 hours before kidney graft reperfusion and at day 4 after kidney transplantation. For pediatric patients weighing > 30kg, the dose of Basiliximab was 20mg, otherwise was 10mg.

Drug: Basiliximab Injection
As an induction treatment for kidney transplantation
Other Names:
  • Simulect
  • rATG induction group

    Rabbit antithymoglobulin (rATG) was administered intravenously during kidney transplantation (pre-reperfusion) and 1-2 days after transplantation. The dose was about 0.5-1 mg/kg per day.

    Drug: rabbit ATG
    As an induction treatment for kidney transplantation
    Other Names:
  • Thymoglobuline
  • Outcome Measures

    Primary Outcome Measures

    1. Acute rejection (AR) [From baseline, kidney transplantation to data collection completion (June 30, 2023)]

      The clinical diagnosis of AR is based on a significant increase in serum creatinine and the exclusion of other causes. The diagnosis of biopsy-confirmed AR is based on relevant histological changes.

    Secondary Outcome Measures

    1. Cytomegalovirus (CMV) viremia [From baseline, kidney transplantation to data collection completion (June 30, 2023)]

      The serum CMV is greater than 500 copies/ml

    2. Pneumonia [From baseline, kidney transplantation to data collection completion (June 30, 2023)]

      Any pneumonia that showed the presence of lesion and required hospitalization

    3. Renal graft survival [From baseline, kidney transplantation to data collection completion (June 30, 2023)]

      The estimated glomerular filtration rate (eGFR) of patient is >15 ml/min/1.73m2

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    1 Month to 18 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Receiving the kidney graft from a deceased donor

    • Basiliximab or rATG induction therapy was used in perioperative period

    Exclusion Criteria:
    • Recipients with pre-transplant calculated panel reactive antibodies (cPRA) >10%

    • Recipients of combined liver, pancreas or heart transplantation

    • No induction or other induction therapy was used in perioperative period

    • Recieving the kidney graft from a living donor

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The First Affiliated Hospital of Sun Yat-sen University. Guangzhou Guangdong China
    2 The First Affiliated Hospital of Zhengzhou University Zhengzhou Henan China
    3 The First Affiliated Hospital of Zhejiang University Hangzhou China
    4 Changhai Hospital affiliated to Naval Military Medical University Shanghai China
    5 Tongji Hospital of Tongji Medical College of Huazhong University of Science and Technology Wuhan China 430030

    Sponsors and Collaborators

    • Gang Chen
    • Zhejiang University
    • First Affiliated Hospital, Sun Yat-Sen University
    • The First Affiliated Hospital of Zhengzhou University
    • Changhai Hospital

    Investigators

    • Principal Investigator: Gang Chen, PhD, Tongji Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Gang Chen, Professor, Tongji Hospital
    ClinicalTrials.gov Identifier:
    NCT06087003
    Other Study ID Numbers:
    • PINK study
    First Posted:
    Oct 17, 2023
    Last Update Posted:
    Oct 17, 2023
    Last Verified:
    Oct 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 17, 2023