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Application of OE in Diagnosis of EGC

Application of OpticalEnhancement Endoscopy(OE) in Diagnosis of Early Gastric Cancer: a Multicenter, Prospective, Randomized Controlled Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04720521
Enrollment
2454
Registered
2021-01-22
Start date
2019-05-10
Completion date
2021-05-10
Last updated
2021-01-22

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

Conditions

High Risk Population of Gastric Cancer

Keywords

early gastric cancer, Optical Enhancement, Detection Rate

Brief summary

The main purpose of this study is to evaluate application value of OE mode 2 in the diagnosis of early gastric cancer The Secondary purpose is to evaluate application value of OE mode 1 in differentiating the diagnosis of neoplastic lesions of the gastric mucosa.

Detailed description

Gastric cancer is the most prevalent cancer in China,while the detection rate of early gastric cancer is lower than 10%. An effective screening method to improve the detection rate is urgently needed. Optical Enhancement (OE) mode is an endoscopic mode that uses the principle of grating for electronic staining, which provides a clear picture of the submucosal and superficial mucosal vascular structures. The OE1 mode provides enhanced images of the gastric Gland tube and blood vessels, as well as magnification. The OE2 mode is used to identify small chromatic aberrations and to visualize superficial structures in the gastric mucosa. So we designed this randomized controlled trial to discuss effectiveness of OE in the diagnosis of early gastric cancer and we hope to find an effective method to improve the detection rate of early gastric cancer in China.

Interventions

DIAGNOSTIC_TESTOE+white light

Firstly use white light to observe from esophagus to duodenum and then switch OE mode to observe from antrum to esophagus

Sponsors

Qilu Hospital of Shandong University
CollaboratorOTHER
Shengjing Hospital
CollaboratorOTHER
Zhengzhou Central Hospital
CollaboratorOTHER
Shanghai Tongji Hospital, Tongji University School of Medicine
CollaboratorOTHER
Tang-Du Hospital
CollaboratorOTHER
Sino-Japanese Friendship Hospital of Jilin University
CollaboratorUNKNOWN
First People's Hospital of Hangzhou
CollaboratorOTHER
Nanjing First Hospital, Nanjing Medical University
CollaboratorOTHER
Peking University Cancer Hospital & Institute
CollaboratorOTHER
The First People's Hospital of Guangzhou
CollaboratorUNKNOWN
First Affiliated Hospital of Guangxi Medical University
CollaboratorOTHER
Tongji Hospital
CollaboratorOTHER
Changhai Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

Meet item 1or 2 + any items of 3-7 1. Male ≥ 40 years old, female ≥ 50 years old. 2. More than one year since the last gastroscopy. 3. Patients from the areas with high incidence of stomach cancer (Shandong Province, Liaoning Province, Fujian Province, Gansu Province, Qinghai Province, Ningxia Province, Jilin Province, Jiangsu Province, Shanghai). 4. Patients with pre-cancerous gastric diseases such as chronic atrophic gastritis, gastric ulcer, gastric polyp, hypertrophic gastritis, pernicious anemia, etc. in the past. 5. First-degree relatives of patients with a family history of gastric cancer. 6. Other high-risk life factors for gastric cancer (high salt, pickled diet, smoking, heavy alcohol consumption, etc.) 7. Positive serum gastric function tests (GastroPanel) include: H. pylori (H.P) antibody (+), Fasting pepsinogen I and II ratio (PG I/PGII) \<3.89, gastrin 17 (G-17) \>1.50 pmol/L.

Exclusion criteria

1. Patients who have undergone invasive treatment such as surgical resection, PEG, chemotherapy etc. of either stomach or oesophagus. (except for EMR and ESD). 2. Patients with a confirmed diagnosis of progressive cancer above T2 degreed according to the TMN classification of cancer。 3. Patients on anticoagulants that cannot be biopsied. 4. Patients who have undergone gastrectomy. 5. Patients who have taken PPIs or H2 receptor antagonist within two weeks. 6. Patients with history of malignant neoplasm; high suspicion of neoplasm; severe cardiac, pulmonary, hepatic or renal insufficiency; severe mental illness and pregnant women. 7. Patients who did not signed the consent form.

Design outcomes

Primary

MeasureTime frameDescription
Detection rate of gastric neoplastic lesionprocedureInclude early gastric cancer, high-grade neoplasia, low-grade neoplasia and adenoma

Secondary

MeasureTime frame
Specificity of detecting gastric neoplastic lesionprocedure
Sensitivity of detecting gastric neoplastic lesionprocedure

Countries

China

Contacts

Primary ContactLiang hao Hu, M.D.
lianghao-hu@hotmail.com8613817593520
Backup ContactDi Zhang, M.D.
hugh_zd@sina.com8613162039421

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026