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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06087003
Other study ID # PINK study
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 3, 2013
Est. completion date September 30, 2023

Study information

Verified date October 2023
Source Tongji Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 958
Est. completion date September 30, 2023
Est. primary completion date July 27, 2022
Accepts healthy volunteers No
Gender All
Age group 1 Month to 18 Years
Eligibility 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

Study Design


Intervention

Drug:
Basiliximab Injection
As an induction treatment for kidney transplantation
rabbit ATG
As an induction treatment for kidney transplantation

Locations

Country Name City State
China The First Affiliated Hospital of Sun Yat-sen University. Guangzhou Guangdong
China The First Affiliated Hospital of Zhejiang University Hangzhou
China Changhai Hospital affiliated to Naval Military Medical University Shanghai
China Tongji Hospital of Tongji Medical College of Huazhong University of Science and Technology Wuhan
China The First Affiliated Hospital of Zhengzhou University Zhengzhou Henan

Sponsors (5)

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

Country where clinical trial is conducted

China, 

References & Publications (8)

Antunes H, Parada B, Tavares-da-Silva E, Carvalho J, Bastos C, Roseiro A, Nunes P, Figueiredo A. Pediatric Renal Transplantation: Evaluation of Long-Term Outcomes and Comparison to Adult Population. Transplant Proc. 2018 Jun;50(5):1264-1271. doi: 10.1016/j.transproceed.2018.02.089. — View Citation

Aw MM, Taylor RM, Verma A, Parke A, Baker AJ, Hadzic D, Muiesan P, Rela M, Heaton ND, Mieli-Vergani G, Dhawan A. Basiliximab (Simulect) for the treatment of steroid-resistant rejection in pediatric liver transpland recipients: a preliminary experience. Transplantation. 2003 Mar 27;75(6):796-9. doi: 10.1097/01.TP.0000054682.53834.EA. — View Citation

Barton KT, Halani K, Galbiati S, Dandamudi R, Hmiel SP, Dharnidharka VR; NAPRTCS investigators. Late first acute rejection in pediatric kidney transplantation: A North American Pediatric Renal Trials and Collaborative Studies special study. Pediatr Transplant. 2021 Aug;25(5):e13953. doi: 10.1111/petr.13953. Epub 2020 Dec 22. — View Citation

Crowson CN, Reed RD, Shelton BA, MacLennan PA, Locke JE. Lymphocyte-depleting induction therapy lowers the risk of acute rejection in African American pediatric kidney transplant recipients. Pediatr Transplant. 2017 Feb;21(1). doi: 10.1111/petr.12823. Epub 2016 Oct 3. — View Citation

Goh HK, Lye WC. Biopsy-proven resolution of steroid-resistant acute rejection with basiliximab therapy in a renal allograft recipient. Transplant Proc. 2001 Nov-Dec;33(7-8):3213-4. doi: 10.1016/s0041-1345(01)02368-5. No abstract available. — View Citation

Martinez-Mier G, Enriquez-De Los Santos H, Mendez-Lopez MT, Avila-Pardo SF, Budar-Fernandez LF, Gonzalez-Velazquez F. Rejection is a strong graft survival predictor in live donor pediatric renal transplantation using cyclosporine, mycophenolate mofetil, and steroids: 5-year outcomes in a single Mexican center. Transplant Proc. 2013 May;45(4):1442-4. doi: 10.1016/j.transproceed.2013.02.044. — View Citation

Mincham CM, Wong G, Teixeira-Pinto A, Kennedy S, Alexander S, Larkins N, Lim WH. Induction Therapy, Rejection, and Graft Outcomes in Pediatric and Adolescent Kidney Transplant Recipients. Transplantation. 2017 Sep;101(9):2146-2151. doi: 10.1097/TP.0000000000001577. — View Citation

Riad S, Jackson S, Chinnakotla S, Verghese P. Primary pediatric deceased-donor kidney transplant recipients outcomes by immunosuppression induction received in the United States. Pediatr Transplant. 2021 Aug;25(5):e13928. doi: 10.1111/petr.13928. Epub 2020 Dec 12. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Acute rejection (AR) 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. From baseline, kidney transplantation to data collection completion (June 30, 2023)
Secondary Cytomegalovirus (CMV) viremia The serum CMV is greater than 500 copies/ml From baseline, kidney transplantation to data collection completion (June 30, 2023)
Secondary Pneumonia Any pneumonia that showed the presence of lesion and required hospitalization From baseline, kidney transplantation to data collection completion (June 30, 2023)
Secondary Renal graft survival The estimated glomerular filtration rate (eGFR) of patient is >15 ml/min/1.73m2 From baseline, kidney transplantation to data collection completion (June 30, 2023)
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