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Development of new diagnostic liquid biopsy technology for ovarian cancer

Development of new diagnostic liquid biopsy technology for ovarian cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500097809
Enrollment
Unknown
Registered
2025-02-26
Start date
2025-03-01
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Ovarian cancer

Interventions

Ovarian Benign Mass Group:None

Sponsors

Second Xiangya Hospital of CSU
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
35 Years to No maximum

Inclusion criteria

Inclusion criteria: Ovarian cancer enrollment criteria: confirmed epithelial OC, such as: serous carcinoma, clear cell carcinoma, endometrioid carcinoma, etc., of which 80% are serous carcinoma and 20% are others. 1. Stage I 40%, Stage II 40%, Stage III 10%, Stage IV 10%; 2. No history of treatment, no surgery, no drug use; 3. > 35 years old; 4. Enrollment criteria for benign ovarian mass group: high-risk samples of ovarian cancer, such as ovarian mass, lump, and cyst. Telephone return visit once every 6 months. If there is a clinical diagnosis, please provide detailed diagnostic information. healthy people; 5.> 35 years old; High-risk populations 1. High-risk samples for ovarian cancer, such as ovarian masses, lumps, cysts. Telephone return visit once in 6 months. If there is a clinical diagnosis, please provide detailed diagnostic information; 2. > 35 years old

Exclusion criteria

Exclusion criteria: 1) Have a history of any cancer except ovarian cancer; 2) Other extraovarian serious diseases, especially major diseases with a survival time of < 3 years; 3) There are factors that affect the diagnostic examination of the disease (e.g., MRI-related pacemaker, ferromagnetic implants, etc.); 4) Known history of allogeneic organ transplantation and allogeneic hematopoietic stem cell transplantation; 5) Known history of primary immunodeficiency; 6) history of blood transfusion within 1 month; 7) Blood draw is risky (e.g., hemophilia, severe anemia - Hb less than 8.0gm/dL); 8) Female patients who are pregnant or trying to become pregnant; 9) Any other condition that, in the opinion of the investigator, may not be suitable for inclusion in the study or may interfere with the completion of the study; 10) Unable to provide informed consent or refuse to draw blood.

Design outcomes

Primary

MeasureTime frame
Whole Genome Methylation Analysis Data;

Countries

China

Contacts

Public ContactFu Chun

Second Xiangya Hospital of CSU

fuchun0814@csu.edu.cn+86 731 85292476

Outcome results

None listed

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