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NCT07842757Not yet recruiting

Preoperative Gastric Volume and High-Risk Gastric Content in Patients With Type 2 Diabetes Mellitus

Clinical and Metabolic Determinants of High Residual Gastric Volume in Patients With Type 2 Diabetes Mellitus

Source: ClinicalTrials.gov · Last updated 30 Sept 2026

Brief summary (registry, in English)

This prospective observational study will evaluate adult patients with type 2 diabetes mellitus who are scheduled for elective surgery. Immediately before preoperative gastric ultrasonography, capillary fasting blood glucose will be measured. Gastric contents will be assessed qualitatively in the supine and right lateral decubitus positions, and residual gastric volume will be estimated using the antral cross-sectional area measured in the right lateral decubitus position. The primary objective is to evaluate the association between fasting capillary blood glucose and the presence of a high-risk stomach. A high-risk stomach will be defined as the presence of solid gastric contents, Perlas Grade 2 gastric contents, or an estimated gastric volume greater than 1.5 mL/kg. Secondary objectives include determining the prevalence of a high-risk stomach and evaluating its associations with demographic characteristics, diabetes-related factors, comorbidities, fasting duration, medication use, gastroparesis-related symptoms, and routine laboratory parameters.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
120 (estimated)
First submitted
21 Sept 2026
Start date
1 Oct 2026
Primary completion date
1 Apr 2027
Lead sponsor
Bakirkoy Dr. Sadi Konuk Research and Training Hospital
NCT number
NCT07842757

What you commit to

  • Study type: Observational
  • Planned participants: 120
  • From 1 Oct 2026 to the primary completion date, 1 Apr 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
  • Systemic opioid or prokinetic drug use within the previous 72 hours

Other illness

  • History of gastric, esophageal, or upper gastrointestinal surgery
  • Anatomical or technical conditions preventing adequate gastric ultrasonographic assessment

Other

  • Pregnancy
  • Body mass index ≥40 kg/m²
  • Presence of a nasogastric tube
  • Known gastroparesis or gastric outlet obstruction
  • Active vomiting
  • Impaired consciousness or inability to provide a reliable medical history
  • Refusal to participate in the study

Who the study is looking for

  • Age 18 years or older
  • Diagnosis of type 2 diabetes mellitus
  • American Society of Anesthesiologists (ASA) physical status II or III
  • Scheduled for elective surgery
  • Suitable for preoperative gastric ultrasonography
  • 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
Bakırköy Dr. Sadi Konuk Training and Research Hospital
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Unknown status

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