Skip to content

Deciphering Epigenetic signatures in Tumor and Exploiting ctDNA study

Deciphering Epigenetic signatures in Tumor and Exploiting ctDNA study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900026080
Enrollment
Unknown
Registered
2019-09-20
Start date
2019-04-01
Completion date
Unknown
Last updated
2019-09-30

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

Conditions

malignant tumor(including breast cancer and esophagus cancer, etc)

Interventions

Malignancy group:none
Control group:none

Sponsors

Cancer Hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Case group: 1. Primary tumor of each organ, multiple malignant tumors of a single organ are considered as a single primary tumor; 2. The tumor must be pathologically sliced or cytologically confirmed to be malignant and not metastasis of other organs; 3. Complete imaging assessment and pathological staging classification; 4. Informed consent from the patient must be obtained prior to starting any study-related procedures and treatments, confirming that the patient is willing to participate in the study and to comply with the research-related requirements. Control group: 1. Complete physical examination assessment to confirms tumor non-existence; 2. Patients with benign tumors need to have complete imaging assessment and histological pathology confirmation; 3. Obtain informed consent from the patient prior to starting any study-related procedures and treatments, confirming that the patient is willing to participate in the study and is subject to research-related requirements.

Exclusion criteria

Exclusion criteria: 1. History of other malignant tumors; 2. Incomplete medical history or imaging data; 3. The patient withdraws from the study due to other physical or social reasons unrelated to the project; 4. Mental illness or other condition that affects patient compliance; 5. Other serious diseases or medical conditions; 6. History of uncontrollable paroxysmal disease, including CNS diseases or mental disorders, and other situations in which investigator determines that the understanding and signing of informed consent might be affected; 7. Those who have undergone blood transfusion or stem cell therapy in the past one year; 8. Any other conditions that the investigator considers inappropriate for the study.

Design outcomes

Primary

MeasureTime frame
ctDNA methylation;

Countries

China

Contacts

Public ContactLiu Jiaqi

Cancer Hospital, Chinese Academy of Medical Sciences

qty14@mails.tsinghua.edu.cn+86 15810263354

Outcome results

None listed

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