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Screening and clinical application value of multi-omics-based tumor early diagnostic markers

Screening and clinical application value of multi-omics-based tumor early diagnostic markers

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200064161
Enrollment
Unknown
Registered
2022-09-28
Start date
2022-09-20
Completion date
Unknown
Last updated
2023-04-17

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

Conditions

Cancer

Interventions

Case series:None

Sponsors

Nanfang Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria for the lung cancer group. 1. Agde at least 18 years; 2. Voluntary signing of the informed consent; 3. Patients diagnosed with lung cancer by the standardized diagnosis of the Chinese Medical Association Clinical Guidelines for the Treatment of Lung Cancer (2022 edition); 4. No other malignant tumors other than lung cancer were confirmed. Inclusion criteria for the gastric cancer group. 1. Agde at least 18 years; 2. Voluntary signing of the informed consent; 3. Patients diagnosed as gastric cancer by the standardized diagnosis of the Chinese Medical Association Clinical Guidelines for the Treatment of Gastric Cancer (2022 edition); 4. No other malignant tumors other than gastric cancer were confirmed. Inclusion criteria for ovarian cancer group. 1. Agde at least 18 years; 2. Voluntary signing of the informed consent; 3. Patients diagnosed as ovarian cancer by the standardized diagnosis of the Chinese Medical Association Clinical Guidelines for the Treatment of Ovarian Cancer (2022 edition); 4. No other malignant tumors other than ovarian cancer were confirmed. Inclusion criteria for healthy individuals group. 1. Agde at least 18 years; 2. Voluntary signing of the informed consent; 3. No significant abnormal physical examination results; 4. No confirmed diagnosis of malignant tumor in the 6 months before enrollment.

Exclusion criteria

Exclusion criteria: Exclusion criteria for the lung cancer group: 1. Inability to collect blood, urine samples, stool samples, cancer and paracancerous tissue; 2. Missing diagnostic or treatment data; 3. Patients who had blood transfusion in the three months prior to enrollment; 4. Pregnant and lactating women. Exclusion criteria for the gastric cancer group: 1. Inability to collect blood, urine samples, stool samples, cancer and paracancerous tissue; 2. Missing diagnostic or treatment data; 3. Patients who had blood transfusion in the three months prior to enrollment; 4. Pregnant and lactating women. Exclusion criteria for the ovarian cancer group: 1. Inability to collect blood, urine samples, stool samples, cancer and paracancerous tissue; 2. Missing diagnostic or treatment data; 3. Patients who had blood transfusion in the three months prior to enrollment; 4. Pregnant and lactating women. Exclusion criteria for the healthy human group: Blood, urine samples, stool samples could not be collected.

Design outcomes

Primary

MeasureTime frame
proteomics;Genomics;metabolomics;

Countries

China

Contacts

Public ContactLei Zheng

Nanfang Hospital of Southern Medical University

nfyyzl@smu.edu.cn+86 13570701908

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026