Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 12:36 AM
Ignite Modification Date:
2025-12-25 @ 12:36 AM
NCT ID:
NCT06759467
Eligibility Criteria:
Inclusion Criteria:
Age: Patients aged 18-75 years. Diagnosis of Gastric Cancer: Histologically confirmed diagnosis of primary gastric cancer, with clinical suspicion of peritoneal metastasis (based on imaging or other clinical findings).
Positive Peritoneal Lavage Cytology (PEC): Patients with suspected PEC-positive gastric cancer, based on previous or current peritoneal lavage cytology results or high clinical suspicion.
ECOG Performance Status: Eastern Cooperative Oncology Group (ECOG) performance status of 0-2, indicating that the patient is well enough to participate in the study and undergo necessary diagnostic procedures.
Informed Consent: Ability and willingness to provide informed consent and comply with the study protocol.
Exclusion Criteria:
Previous Cancer History: History of other malignancies within the past 5 years, except for non-melanoma skin cancer or in situ cancers.
Severe Comorbidities: Severe cardiovascular, respiratory, renal, or hepatic disease that would impair the patient's ability to participate in the study or undergo the required diagnostic procedures.
Pregnancy or Lactation: Pregnant or breastfeeding women, or women planning to become pregnant during the study period.
Non-Eligible Clinical Conditions: Any condition that, in the opinion of the investigator, could interfere with the patient's participation or compliance with the study protocol, or affect the quality of the data.
Inability to Provide Samples: Patients who are unable to provide the necessary clinical samples (e.g., blood, urine, or peritoneal lavage fluid) for the AI-driven virtual biopsy analysis.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT06759467
Study Brief:
Protocol Section:
NCT06759467