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A Multicenter, Prospective Blood Collection Study in a Kidney Transplant Population

RecruitingObservational study

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

1. Willing and able to provide written informed consent
2. Is 18 years of age or older at enrollment
3. Had a kidney transplant prior to enrollment
4. Is having an indication (for cause) biopsy as determined by clinician
5. retrospective leftover samples are available from the kidney donor(s).

Exclusion Criteria:

1. Is pregnant
2. Had a blood transfusion within the past 4 weeks
3. Had a transplant from an identical (monozygotic) twin
4. Had transplants of multiple organs from the same donor (eg, kidney and liver transplant).
5. Had transplants of more than 2 organs from different donors (eg, recipient of a third kidney transplant)
6. Had a transplant of hematopoietic stem cells (eg, bone marrow) or tissue (eg, heart valve)

About the study

The purpose of this research is to collect blood samples and data from kidney transplant patients. The samples and data will be used for research and development of non-invasive test to detect donor-derived cell-free DNA (dd-cfDNA) in kidney transplant patients to evaluate the status of the transplanted organ.

Sponsor: Devyser Inc. · Participants: 400 · Started: Nov 14, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT07006831

Locations in the U.S.

CaliforniaScripps Health, San Diego
University of California San Francisco, San Francisco
GeorgiaPiedmont Healthcare, Atlanta
MarylandUniversity of Maryland Baltimore, Baltimore
MassachusettsBrigham & Women's Hospital, Boston

Conditions

From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.