Actively Recruiting

Age: 0 - 17Years
All Genders
ID06754709

Evaluation of the Levels of O-GlcNAcylation of Cardiac and Blood Proteins in Pediatric Cardiac Surgery and Identification of Therapeutic Targets

Led by Nantes University Hospital · Updated on 2025-04-13

300

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Cardiac surgery in children often requires the use of extracorporeal circulation (ECC), which can cause significant inflammatory responses and organ injury, especially in younger or smaller patients. This research focuses on studying the levels of O-GlcNAcylation, a protein modification involved in cellular metabolism and stress adaptation, as a potential therapeutic target to improve heart and endothelial function after cardiac surgery. The study aims to better understand how O-GlcNAcylation changes during surgery and its relation to patient outcomes. Children aged 0 to 17 years undergoing cardiac surgery with ECC will participate in this observational study. Blood samples and, if available, cardiac tissue removed during surgery will be collected for analysis alongside routine medical care. The study will measure O-GlcNAcylation levels from the start of surgery to 12 hours after, using Western blot analysis on samples collected during and after the operation. Medical and administrative data will be collected retrospectively from patient records. Participants will be monitored as part of the post-operative cardiac surgery network, with data collected up to six years after surgery to explore links between O-GlcNAcylation levels and long-term prognosis. This study involves regular blood sampling during surgery and retrospective review of health records, without altering standard treatment. The goal is to identify new therapeutic targets to reduce complications like low cardiac output and organ dysfunction following ECC in children.

CONDITIONS

Brief Title

Evaluation of Blood and Cardiac Protein O-GlcNAcylation Levels in Cardiac Surgery in Children

Who Can Participate

Age: 0 - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age from 0 to 17 years at the time of sampling
  • Children undergoing extracorporeal circulation for cardiac surgery
  • Signed bio-collection consent
Not Eligible

You will not qualify if you...

  • Children with an infection
  • Children with fever
  • Children with an immune deficiency
  • Children with autoimmune disease
  • Children with metabolic disease
  • Children with hematological diseases
  • Children with a genetic disease
  • Unsigned consent
  • Refusal by parents or child

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - From start of surgery to 12 hours after start of surgery

Participants undergo cardiac surgery with extracorporeal circulation. Blood samples and, if planned, cardiac tissue samples are collected during and shortly after surgery.

Surgery day and immediate post-operative monitoring

Long-term Monitoring

Duration - Up to 6 years after inclusion

Participants are monitored retrospectively through medical records and followed for prognosis analysis up to 6 years after surgery.

Data collected retrospectively; no additional visits required

Trial Site Locations

Total: 1 location

1

Nantes University Hospital

Nantes, France

Actively Recruiting

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Research Team

M

Manon Denis

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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