The First Affiliated Hospital with Nanjing Medical University
Phase
Observational
Started
2021-11-01
Last updated
2024-10-15
Condition(s) studied
Gastric Cancer Stage
Investigational drug(s) / intervention(s)
DECT examinationmpMRI examination
DECT examination: DECT examinations will be performed using a 192-slice CT scanner (SOMATOM, Force, Siemens, Forchheim, Germany).
mpMRI examination: The examinations were conducted on a 3-T MR scanner (MAGNETOM Skyra; Siemens Healthcare, Erlangen, Germany).
Study summary
Accurate preoperative staging of gastric cancer is of major importance for guiding therapeutic decision-making, preventing both under- and over-treatment. The purpose of this study is to investigate the diagnostic performance of the Multi-parametric magnetic resonance imaging (mpMRI) and dual-energy computed tomography (DECT) in gastric cancer.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Consecutive patients with preoperative pathologically confirmed GC by endoscopy and preoperative imaging data (DECT/mpMRI) were included.
* No contraindications for CT/MRI examination
* Written informed consent
Exclusion Criteria:
* Patients with a history of previous therapy.
* Patients with recurrent gastric cancer
* Patients with a history of severe allergy to contrast agents
* Patients with imaging artefacts affect the evaluation
Primary outcome measure(s)
Diagnostic performance of DECT and mpMRI in tumor staging assessment — 2 years Accuracy for both imaging techniques in the prediction of tumor staging.
Diagnostic performance of DECT and mpMRI in tumor restaging assessment — 2 years Accuracy for both imaging techniques in the prediction of tumor restaging.
Trial sites (1)
Facility
City
Region
Status
Yu-Dong Zhang
Nanjing
China
Recruiting
More The First Affiliated Hospital with Nanjing Medical University trials in China
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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