Study Of Ultrasound Windows For Measuring Inferior Vena Cava Changes Before Cardiac Surgery

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorSunnybrook Health Sciences Centre

About this trial

This research study will compare two ultrasound methods for assessing the inferior vena cava (IVC), a major vein that reflects intravascular fluid status and cardiac function before and after surgery. The standard method uses a subcostal ultrasound view obtained below the breastbone, but this approach may be limited in patients with obesity, surgical dressings, or postoperative discomfort. An alternative approach, the transhepatic view, uses the liver as an acoustic window and may provide improved feasibility in these situations.

The study will evaluate whether the transhepatic view provides measurements comparable to the standard subcostal view and whether operators with different levels of ultrasound experience obtain consistent results using both methods. Adult patients who are awake and scheduled for cardiac surgery at Sunnybrook Health Sciences Centre will undergo a brief ultrasound examination before surgery. The scan takes less than 10 minutes, involves no discomfort, and does not alter clinical care. This is a minimal-risk observational study with no therapeutic interventions. Participation is voluntary, and all personal health information will remain confidential. Findings may inform future approaches to ultrasound-guided assessment and training in perioperative care.

Eligibility criteria

Qualifiers

Adults aged eighteen years or older

Scheduled to undergo cardiac surgery at Sunnybrook Health Sciences Centre

Spontaneously breathing at the time of ultrasound assessment

Able to lie supine for image acquisition

Disqualifiers

Inability to lie supine

Known right heart failure

Moderate to severe tricuspid regurgitation

Portal hypertension

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

283 Participants
are grouped into 1 trial group