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Transabdominal Gastric Contrast Ultrasound

Application Value of Transabdominal Gastric Contrast Ultrasound in the Diagnosis and Staging Evaluation of Gastric Cancer

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05596864
Enrollment
1000
Registered
2022-10-27
Start date
2022-12-01
Completion date
2024-12-30
Last updated
2022-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Transabdominal Gastric Contrast Ultrasound

Brief summary

In this study, the clinical data of patients diagnosed with gastric cancer who were ready for surgery were examined by contrast-enhanced ultrasonography and gastric-enhanced CT before surgery. Based on the results of postoperative pathological examinations, the diagnostic accuracy of gastric filling contrast-enhanced ultrasonography and gastric contrast-enhanced CT in different stages of gastric cancer was compared and analyzed. Provide better guidance for follow-up clinical practice.

Interventions

DIAGNOSTIC_TESTgastric contrast ultrasound

Gastric contrast ultrasound (GCUS) refers to that the patient fills the stomach cavity with oral water, contrast agent and ultrasound contrast agent before the examination to remove the gas in the stomach cavity and fill the stomach cavity to become a homogeneous echo area and form a good acoustic sound. Interface contrast, more clearly showing the gastric wall hierarchy and the ultrasound examination method of the lesions. In this way, not only the changes of the gastrointestinal mucosa can be found, but also the submucosal tumors of the gastrointestinal tract can be clearly displayed, the internal structural characteristics of the tumor, the extent of the lesions, the depth of infiltration, the TNM staging of the tumor, and the lesions of the surrounding organs can be displayed.

Sponsors

The First Hospital of Jilin University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Age: 18\ 80 years old, male or female; 2. Diagnosed with gastric cancer by histology or cytology; 3. No distant multiple metastasis; 4. ECOG score 0-2; 5. Heart, lung, liver and kidney function can tolerate surgery; 6. Patients and their families can understand and be willing to participate in this clinical study, and sign the informed consent.

Exclusion criteria

1. Previous history of malignant tumor or recent diagnosis combined with other malignant tumors; 2. Patients with gastrointestinal perforation, gastrointestinal bleeding, etc. requiring emergency surgery; 3. Patients with previous gastroduodenal surgery; 4. Preoperative neoadjuvant therapy; 5. Patients and their families refuse surgical treatment; 6. ASA grade ≥ IV and/or ECOG performance status score \> 2; 7. Patients with severe liver and kidney function, cardiopulmonary function, coagulation dysfunction or combined with serious underlying diseases who cannot tolerate surgery; 8. Have a history of serious mental illness; 9. Pregnant or lactating women; 10. Patients with other clinical and laboratory conditions considered by the researchers should not participate in this trial.

Design outcomes

Primary

MeasureTime frame
Sensitivity, specificity and accuracy of gastric contrast ultrasound in judging gastric cancer staging.one month after surgery

Contacts

Primary ContactWei Li, Prof.
weili8308@126.com13596157865

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026