Skip to content

Evaluation of Pro-Inflammatory Leukocyte Activity in Patients Undergoing Cardiac Surgery

Evaluation of Pro-Inflammatory Leukocyte Activity in Patients Undergoing Cardiac Surgery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04299828
Enrollment
100
Registered
2020-03-09
Start date
2022-05-31
Completion date
2026-12-31
Last updated
2026-01-07

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

Conditions

Coagulation, Congenital Heart Disease

Brief summary

The goal of this proposal is to prospectively collect data from a series of 200 patients (all ages) undergoing complex cardiac surgical procedures involving cardiopulmonary bypass (CPB) to: 1. Measure the number of blood activated circulating monocytes before, during and after cardiac surgery and serum GABA and pro-inflammatory cytokine levels 2. Understand the correlation between GABA and inflammatory cytokines (and/or activated monocytes) and 3. Assess the correlation between thrombosis and monocyte activation in patients undergoing cardiac surgery under CPB and at risk of thrombosis.

Detailed description

Often when people undergo heart surgery, they are placed on cardiopulmonary bypass (CPB). Sometimes clotting of the blood occurs during and after heart surgery with CPB, which can lead to multiple complications. In order to try to avoid abnormal/excessive clotting that may lead to complications, it is important to understand the specific causes of why the blood sometimes clots abnormally during and after heart surgery. Currently, tests looking at how the blood clots (coagulation assessment) are usually performed as standard laboratory testing during and after surgery. However, these tests are not able to predict the future development of abnormal clots. This study will be looking at the role that immune cells (monocytes) have in the formation of abnormal clots after heart surgery. It is possible that these immune cells produce signals that can contribute to the formation of clots. Using experimental tests (monocyte analysis and mediator analysis), the hope is to understand if these cells participate in forming abnormal clots in any meaningful way. Although these tests are not yet approved for use in children, this study plans to use these new methods to understand this phenomenon by analyzing the blood at different times during the surgery and recovery period. Overall, the purpose of this study is to look at these tests in people undergoing heart surgery to help the investigators understand why the blood sometimes forms clots abnormally. Results from this study may help treat future patients who experience abnormal clotting during and after surgery.

Interventions

Will utilize the discarded blood from routine clinical blood samples to evaluate the role of immune cells in coagulopathy.

Sponsors

Boston Children's Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients (all ages) undergoing complex cardiac surgical procedures with CPB.

Exclusion criteria

* undergoing an emergent procedure and do not have more than 1 hour ahead of time to review the consent * patient in a moribund condition American Society of Anesthesiology (ASA 5) -patient with a hematological and/or oncological disease * Jehovah witnesses.

Design outcomes

Primary

MeasureTime frameDescription
Monocyte activation statusThrough study completion; on average one yearcharacterization of monocyte activation status at baseline before surgery and throughout the course of CPB including post-operatively.
Serum GABA and pro-inflammatory cytokinesThrough study completion; on average one yearSerum GABA and pro-inflammatory cytokines

Secondary

MeasureTime frameDescription
Clinical ThrombosisThrough study completion; on average one yearPresence of clinical thrombosis

Countries

United States

Contacts

Primary ContactKoichi Yuki, MD
koichi.yuki@childrens.harvard.edu617-355-6225
Backup ContactRachel Bernier
Rachel.Bernier@childrens.harvard.edu857-218-5348

Outcome results

None listed

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