Gastric Cancer Clinical Trial
Official title:
Early Detection and Post-operative Monitoring of Gastric Cancer Using Circulating DNA in Blood Samples
Verified date | January 2024 |
Source | SUZHOU HUHU HEALTH & TECHNOLOGY Inc., |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
This study is to determine the performance of non-invasive new multi-target biomarkers in the early detection and post-operative monitoring of gastric cancer.
Status | Recruiting |
Enrollment | 1197 |
Est. completion date | February 17, 2026 |
Est. primary completion date | February 17, 2026 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: 1. Subject age over 18. 2. Subject has stomach discomfort, and seek medical attention at the Gastric Surgery Department of our center. 3. Subject has or will have gastroscopy and/or pathological examination results at this center. 4. Subject must be able to fully understand the informed consent form and be able to personally sign it. Exclusion Criteria: 1. Subject has serious heart, liver, kidney dysfunction, or mental illness. 2. Subject diagnosed previously with any kind of malignant tumor. 3. Subject is known to be infected with HIV or other related diseases (considering interference from the use of immune drugs). 4. Subject is receiving targeted drugs, immunosuppressants, immunomodulators, and biological therapies. 5. Researchers believe that subject is not suitable for enrollment. 6. Subject can not supply sufficient sample to complete this experiment. |
Country | Name | City | State |
---|---|---|---|
China | Fudan University Shanghai Cancer Center. | Shanghai | Shanghai |
China | Fudan University Shanghai Cancer Center. | Shanghai | Shanghai |
Lead Sponsor | Collaborator |
---|---|
SUZHOU HUHU HEALTH & TECHNOLOGY Inc., | Fudan University |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The performance of the new detection system for gastric cancer (GC) detection | Evaluate sensitivity, specificity, accuracy, ROC curve area, positive predictive value, and negative predictive value of the new biomarker for the diagnosis of gastric cancer. | 2 years | |
Primary | The performance of the new biomarkers in the post-operative monitoring of gastric cancer | Determine whether the new detection system can detect tumor recurrence and metastasis earlier than imaging and tumor marker CA19-9, CEA, and CA72-4. | 2 years | |
Secondary | Compare the performance of the new biomarkers for GC detection with the conventional tumor markers | Determine whether the performance of the new biomarker detection system is better than that of tumor markers CA19-9, CEA, and CA72-4 in the diagnosis of gastric cancer. | 2 years | |
Secondary | The performance of the new biomarkers as prognostic biomarkers | Determine whether the new biomarkers cancer serve as prognostic biomarkers to predict tumor recurrence and metastasis. | 2 years |
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