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Sleep Quality and Sleep-disordered Breathing in Bypass Surgery Patients (UNI-CABG)

T

Turku University Hospital (TYKS)

Status

Enrolling

Conditions

Coronary Artery Disease
Sleep Disorder

Study type

Observational

Funder types

Other

Identifiers

NCT06453538
27 /1801/2022

Details and patient eligibility

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

Full description

Detailed Description:

Our hypothesis is that sleep-related apneas are increasing following coronary artery bypass surgery, and sleep quality may deteriorate. We are attempting to determine the causes of these difficulties, which are caused by microemboli in the brain from the use of a heart-lung machine, brain infarction induced by major surgery, thoracic tissue trauma following surgery, or complications during perioperative care. The hypothesis is that postoperative outcomes and recovery are related if a patient is identified with sleep apnea before CABG surgery. A sleep polygraph is performed before surgery and again around six months after, as well as a transthoracic echo and laboratory tests. If a link between sleep quality and coronary bypass surgery can be established, the results can be employed in clinical practice.

The total amount of patients operated on heart-lung machine is anticipated to be 70. The off-pump patient sample size is remarkably smaller, so data is collected and compared with the main sample population. The operation technique is decided when the patient is scheduled for operation. Emergency patients are excluded because pre-operative examinations cannot be performed. Other exclusion criteria are nighttime CPAP- treatment and other heart operations (for example valve surgery) during CABG.

Basic information including age, weight, height, diseases, medications, and medical history are collected from all patients. ECG is registered before and after surgery and sinus or other heart rhythms are recorded. Sleep polygraph is done preoperatively and postoperatively when the patient is fully recovered from surgery (at 6 months or more).

Enrollment

54 estimated patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Elective coronary artery bypass surgery

Exclusion criteria

  • Emergency cabg
  • Night time cpap- treatment
  • other heart operations (for example valve surgery)

Trial contacts and locations

1

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Central trial contact

Marjo Ajosenpää, MD; Jenni Toivonen, millä Associate Professor

Data sourced from clinicaltrials.gov

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