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Liquid Biopsies for minimally invasive Detection of Acute Rejection

Liquid Biopsies for minimally invasive Detection of Acute Rejection - LIBIDAR

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON50673
Enrollment
450
Registered
2018-04-24
Start date
2018-08-15
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

orgaantransplantatie graft rejection transplant rejection

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Adult kidney transplant recipients (>= 18 years of age) receiving a kidney transplant of either a living or deceased donor in the Erasmus MC.

Exclusion criteria

Exclusion criteria: Below 18 years of age

Design outcomes

Primary

MeasureTime frame
Primary endpoint of this explorative study is the ability to identify kidney allograft rejection by markers in blood and/or urine; i.e. level of dd-cfDNA, presence of specific nucleosome variants, circulating endothelial cells and the presence of EVs. Therefore, the outcome of the proposed markers will be correlated with the currently used methods which are the kidney biopsy, serum creatinine and urinary protein concentrations.

Secondary

MeasureTime frame
Secondary the proposed markers will be correlated with the urinary concentrations of CXCL9 and CXCL10, which are promising upcoming non-invasive markers for allograft rejection. In exploratory analyses, we will try to identify the best marker or combination of markers to diagnose kidney transplant rejection.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Aug 9, 2026