Application of CfDNA Methylation Detection in Auxiliary Diagnosis of Breast Cancer
Recruiting
Observational Study
Breast Cancer Screening
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
30 – 75
Sex
Any
Study type
Observational
Participants needed
200 (estimated)
Sponsor
Geneplus-Beijing Co. Ltd. · Industry
Who this trial is looking for
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
The purpose of this study is to construct an auxiliary diagnostic model for breast cancer by methylation markers. The study will collect blood and tissue samples from participants with breast cancer and benign disease for whole-genome methylation sequencing. It will screen methylation markers and develop a methylation auxiliary diagnosis model to distinguish between breast cancer and non-cancer.
Trial Locations
Loading…
Loading trial locations…
Facility
City
State
Country
Status
Eligibility Criteria
Inclusion Criteria for All the Participants:
* With confirmed pathological diagnosis and molecular subtyping results
* Ability to provide a written informed consent
Exclusion Criteria for Cancer Arm Participants:
* Patients with a history of or currently suffering from other malignancies
* Pregna…
Inclusion Criteria for All the Participants:
* With confirmed pathological diagnosis and molecular subtyping results
* Ability to provide a written informed consent
Exclusion Criteria for Cancer Arm Participants:
* Patients with a history of or currently suffering from other malignancies
* Pregnant or planning to become pregnant female patients
* Patients who have received cancer treatment, including surgery, chemotherapy, radiotherapy, targeted therapy, and immunotherapy, before blood draw
* Patients with a history of blood transfusion within the past month
* Patients with a known history of allogeneic organ transplantation and allogeneic hematopoietic stem cell transplantation
* Patients with persistent fever or undergoing anti-inflammatory treatment within 14 days before blood draw
* Any other conditions that the researcher deems may make the patient unsuitable for inclusion in the study or may interfere with the completion of the study
* Patients in poor physical condition who are not suitable for blood draw
* Patients who cannot provide informed consent or refuse blood draw
Exclusion Criteria for Benign Diseases Arm Participants:
* History of malignancies
* Current malignancies or precancerous lesions
Contacts
No contact information available.
What are you hoping to find?
Picking one helps us show the most relevant trials first.
Your results are loading in the background — you can
change this any time from the results page.
Set your location to continue
Find My Trials uses your location to surface clinical trials near you.
Add your city or zip code to your profile and try again.