Actively Recruiting
Sleep Quality and Sleep-disordered Breathing in Bypass Surgery Patients
Led by Turku University Hospital · Updated on 2024-06-26
54
Participants Needed
1
Research Sites
151 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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
Official Title
Sleep Quality and Sleep-disordered Breathing in Bypass Surgery Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Elective coronary artery bypass surgery
You will not qualify if you...
- Emergency coronary artery bypass surgery
- Nighttime CPAP treatment
- Other heart operations during coronary bypass surgery (for example valve surgery)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Turku University Hospital
Turku, Finland, 20720
Actively Recruiting
Research Team
M
Marjo Ajosenpää, MD
CONTACT
J
Jenni Toivonen, millä Associate Professor
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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