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ABO-Incompatible Kidney Transplants Between Robot-Assisted vs. Open Surgery

A Comparative Study on Outcomes of ABO-Incompatible Kidney Transplants Between Robot-Assisted vs. Open Surgery: A Retrospective Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06287008
Enrollment
239
Registered
2024-02-29
Start date
2020-10-01
Completion date
2024-01-31
Last updated
2024-03-01

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

Conditions

Kidney Transplantation

Keywords

robot-assisted kidney transplantation, ABO incompatible, biopsy-proven acute rejection, immunologically high-risk patients

Brief summary

While robot-assisted kidney transplantation (RAKT) offers potential benefits such as minimal postoperative pain, better cosmesis, fewer wound infections, and shorter hospital stay, its efficacy in ABO-incompatible (ABO-i) KT compared to open KT (OKT) remains understudied. This study aims to compare ABO-i KT outcomes between RAKT and OKT. The study utilized data from 29 ABO-i RAKT and 210 ABO-i OKT cases performed at Asan Medical Center from October 2020 to February 2023. Univariate and multivariate analyses were performed to evaluate factors associated with a composite of biopsy-proven acute rejection (BPAR), de novo donor-specific antibodies (DSA), and overall graft failure.

Interventions

The interventional surgery is a robot-assisted kidney transplantation and its efficacy will be measured against that of open kidney transplantation

Sponsors

Asan Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patient eligible for living donor ABO incompatible kidney transplantation * Presenting an IsoAgglutinin immunoglobulin G titer (anti-A-B) between 1/8 and 1/128 before operation * Patient older than 18 years and young than 80 years * Patient able to sign an informed consent form

Exclusion criteria

* Patient with comorbidities or hypersensitivity that prevent desensitization protocols * Women who are pregnant, or who may become pregnant or breastfeeding women * Subjects under legal protection * Subjects participating in another interventional research protocol or in an exclusion period from another interventional research protocolPatient affiliated with a social security scheme

Design outcomes

Primary

MeasureTime frameDescription
Graft survival1 year post-operativeallograft (kidney) survival
renal function1 year post-operativerenal function measured in terms of eGFR (Estimated Glomerular Filtration Rate)

Secondary

MeasureTime frameDescription
. A composite of biopsy-proven acute rejection, graft failure, and the development of de novo donor-specific antibodies1 year post-operative. A composite of biopsy-proven acute rejection, graft failure, and the development of de novo donor-specific antibodies

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026