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Measurement of Circulating Cell-free DNA (cfDNA) for Diagnosis and Prognosis of Various Diseases and Evaluation of Tissue Damage

Development of a Fast and Sensitive Method for Measurement of Circulating Cell-free DNA (cfDNA) for Diagnosis and Prognosis of Various Diseases and Evaluation of Tissue Damage Following Trauma

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05094960
Enrollment
71
Registered
2021-10-26
Start date
2009-07-30
Completion date
2021-07-30
Last updated
2021-11-05

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

Conditions

Correlation of cFDNA During CPB to Laboratories SIRS Parameters and Clinical Outcomes

Keywords

cfDNA-Circulating cell-free DNA, CPB-cardiopulmonary bypass, SIRS-systemic inflammatory response syndrome

Brief summary

To characterize the changes in circulating cell-free DNA (cfDNA) levels during cardiopulmonary bypass (CPB) and to access their association with outcomes compared to standard scores.

Detailed description

In a prospective study, the investigators enrolled seventy-one consecutive patients undergoing non-emergent coronary artery bypass grafting. Blood was drawn at baseline, after 20 and 40 minutes on CPB, after cross-clamp removal, and 30 minutes after chest closure. cfDNA was measured in sera by fluorescent method. The investigators hypothesize that cfDNA measured by will reflect the magnitude of inflammation induced by CPB. Thus, these measurements could serve for the real-time prognosis of patients undergoing cardiac surgery. The investigators correlate cFDNA to laboratories and clinical outcomes.

Interventions

DIAGNOSTIC_TESTBlood samples

5 blood samples for each patient during CABG (coronary artery bypass grafting) surgery pre/on/post cardiopulmonary bypass machine

Sponsors

Soroka University Medical Center
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Elective coronary artery bypass grafting surgery

Exclusion criteria

* Age \< 18 * Non elective surgery * other than CABG surgery * Redo CABG

Design outcomes

Primary

MeasureTime frameDescription
prolong LOS-length of stay> 18 hours after the surgeryintensive care unit length of stay
Mortalityshort term - 30day; long term > 1yearMortality

Secondary

MeasureTime frameDescription
Neutrophil-NETosis2 hours after the surgeryNeutrophil extracellular traps (NETs) released from activated neutrophils that undergo NETosis.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026