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Detection of potential biomarkers CXCL9, CXCL10, CCL2, CCL 5, IL-37 and IL-38 in blood and urine for acute and chronic rejection after kidney transplantation

Detection of potential biomarkers CXCL9, CXCL10, CCL2, CCL 5, IL-37 and IL-38 in blood and urine for acute and chronic rejection after kidney transplantation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00015435
Enrollment
250
Registered
2018-11-07
Start date
2018-11-12
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

T86.1

Interventions

Group 1: Investigation of serum and urine among patients with kidney allograft without rejection and without CMV- or BKV-infection on one examination day Group 2: Investigation of urine and serum amon

Sponsors

Klinikum der Johann Wolfgang Goethe-Universität Frankfurt am Main
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Group A: Men and women over the age of 18, who receive a kidney allograft and have no signs for rejection. The earliest inclusion date is four weeks after kidney transplantation. Group B: Men and women over the age of 18, who receive a kidney allograft and have a rejection, which is confirmed by a kidney biopsy Group C: Men and women over the age of 18, who receive a kidney allograft and suffer from a CMV- or BKV-infection Group D: Men and women over the age of 18, after de novo kidney transplantation Group K: Healthy men and healthy women over the age of 18, who don’t receive a kidney allograft

Exclusion criteria

Exclusion criteria: exclusion criteria arise from inclusion criteria

Design outcomes

Primary

MeasureTime frame
Primary endpoint of the study is the recording of the concentrations of the following molecules in the blood and urine of the study participants: CXCL9, CXCL10, CCL2, CCL5, IL-37 and IL-38. If additional potential biomarkers are investigated among the study participants, the recording of the concentrations of these additional potential biomarkers will be the primary endpoint.

Secondary

MeasureTime frame
non-existent

Countries

Germany

Contacts

Public ContactIngeborg A. Hauser

Medizinische Klinik III - Funktionsbereich Nephrologie Universitätsklinikum Frankfurt

ingeborg.hauser@kgu.de069/6301-6668

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026