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NCT07898215Not yet recruiting

Preoperative Gastric Ultrasound and Left Ventricular Function in Coronary Artery Bypass Surgery

Evaluation of the Relationship Between Preoperative Gastric Ultrasonography Findings and Left Ventricular Systolic Function in Patients Undergoing Elective Coronary Artery Bypass Graft Surgery

Source: ClinicalTrials.gov · Last updated 30 Oct 2026

Brief summary (registry, in English)

This study aims to investigate whether reduced heart function is associated with differences in stomach contents before elective coronary artery bypass graft (CABG) surgery. Patients undergoing elective cardiac surgery will be divided into two groups based on their left ventricular ejection fraction (LVEF), a measure of how well the heart pumps blood: patients with an LVEF below 40% and patients with an LVEF of 40% or higher. Before surgery, the researchers will use ultrasound to examine the stomach. They will assess the presence and amount of stomach contents using the Perlas grading system and ultrasound measurements of the gastric antrum. The main objective is to compare gastric ultrasound findings between the two groups. The researchers will also evaluate estimated gastric volume and the frequency of stomach findings associated with a higher risk of aspiration during anesthesia.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
50 (estimated)
First submitted
21 Oct 2026
Start date
1 Nov 2026
Primary completion date
1 Mar 2027
Lead sponsor
Adiyaman University
NCT number
NCT07898215

What you commit to

  • Study type: Observational
  • Planned participants: 50
  • From 1 Nov 2026 to the primary completion date, 1 Mar 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Emergency surgery.

Other illness

  • History of upper gastrointestinal surgery.
  • Known gastroparesis or severe gastrointestinal motility disorders.
  • History of gastroesophageal reflux disease (GERD).

Other

  • Active nausea or vomiting.
  • Body mass index (BMI) \>40 kg/m².
  • Inability to cooperate with gastric ultrasonography assessment.
  • Refusal to participate in the study.

Who the study is looking for

  • Age ≥18 years.
  • Scheduled for elective coronary artery bypass grafting (CABG) surgery with cardiopulmonary bypass.
  • Willingness to participate in the study and provision of written informed consent.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Adıyaman Training and Research Hospital
Coordinator of this site? Confirm its status
AdıyamanTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.