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Sleep Quality and Sleep-disordered Breathing in Bypass Surgery Patients

NCT06453538 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 54

Last updated 2024-06-26

No results posted yet for this study

Summary

Patients undergoing non-emergency coronary artery bypass surgery (CABG) are included. All patients will be examined for transthoracic echo, blood samples will be collected, and an overnight sleep polygraph will be performed in a qualified sleep laboratory twice: once before CABG and again after surgery

Conditions

Sponsors & Collaborators

  • Turku University Hospital

    lead OTHER_GOV

Principal Investigators

  • Nea Kalleinen, millä Associate Professor · Turku University Hospital/Heart Center

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-02-01
Primary Completion
2025-12-30
Completion
2025-12-30

Countries

  • Finland

Study Locations

More Related Trials

Entities

Diseases

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 NCT06453538 on ClinicalTrials.gov