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Neuroinflammation/Oxidative Stress/Cardiac Surgery

Assessing Neuroinflammation and Oxidative Stress After Cardiac Surgery: Unveiling Molecular Dynamics and Clinical Outcomes

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06391866
Acronym
NEuOX-postSURg
Enrollment
60
Registered
2024-04-30
Start date
2024-04-30
Completion date
2025-12-31
Last updated
2024-04-30

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

Conditions

Neuroinflammation

Brief summary

The prospective observational study delves into the complex relationship between neuroinflammation and oxidative stress in post-cardiac surgery complications, focusing on postoperative cognitive dysfunction.

Detailed description

The prospective observational study meticulously examines the interplay between neuroinflammation and oxidative stress in the realm of post-cardiac surgery complications, specifically targeting postoperative cognitive dysfunction. Its primary objective is to comprehensively assess the sustained influence of these intricate processes on cognitive function and overall well-being, extending beyond the immediate aftermath of surgery. The research endeavors to probe deeply into the molecular mechanisms and clinical ramifications associated with neuroinflammation and oxidative stress, centering on their pivotal role in shaping the onset and trajectory of postoperative cognitive dysfunction.

Interventions

OTHERextracorporeal circulation

extracorporeal circulation during cardiosurgical operation

Sponsors

East Slovak Institute for Cardiovascular Diseases
CollaboratorOTHER
Europainclinics z.ú.
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years

Inclusion criteria

* Undergoing cardiosurgical operation * Absence of previous neurological disease * Signed informed consent document

Exclusion criteria

* Presence of neoplasms * Neurological Disease * Refusal to participate in the clinical trial

Design outcomes

Primary

MeasureTime frameDescription
Number and type of early complications after surgery1 monthEstimating of postoperative complications
Number and type of postoperative complications6 monthsEstimating of postoperative complications

Secondary

MeasureTime frameDescription
Estimating biochemical parameters1 hourPro-inflammatory interleukins parameters (e.g. IL-8, IL-6, MIP-1a, MMP-2, MMP-9, SIRT 1, SIRT 2)
Estimating biochemical parameters Third biochemical examination1 hourAntioxidative enzymes

Countries

Slovakia

Contacts

Primary ContactLadislav Kočan, MD, PhD, FIPP
europainclinicsstudy@gmail.com+421557891110
Backup ContactJanka Vašková, prof. Dr. PhD.
janka.vaskova@upjs.sk

Outcome results

None listed

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