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Five Years Follow-up of Neurological Outcome After Minimally Invasive Cardiac Surgery

NCT05330260 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 55

Last updated 2023-03-08

No results posted yet for this study

Summary

A monocenter observational study will be started to investigate postoperative cognitive dysfunction 5 years after minimally invasive cardiac surgery. Postoperative cognitive dysfunction will be evaluated in three groups: an endoscopic-CABG group (endo-CABG), a PCI (Percutaneous Coronary Intervention) group and a healthy control group. It is hypothesized that the endo-CABG group will show a stronger postoperative cognitive dysfunction compared to the PCI group and the healthy control group.

Conditions

  • Surgery
  • Postoperative Cognitive Dysfunction

Interventions

DIAGNOSTIC_TEST

neurocognitive test battery

Assessment of the incidence of late postoperative cognitive decline (LPOCD)

Sponsors & Collaborators

  • Jessa Hospital

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-03-25
Primary Completion
2022-11-07
Completion
2022-11-07

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05330260 on ClinicalTrials.gov