Eligibility Module

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: 2025-12-24 @ 4:49 PM
Ignite Modification Date: 2025-12-24 @ 4:49 PM
NCT ID: NCT05667350
Eligibility Criteria: Inclusion Criteria for Cancer Arm Participants: * Age 40-75 years at the day of consenting to the study. * Able to provide a written informed consent * Pathologically confirmed biliary tract cancers. * No prior or ongoing anti-cancer therapy (local or systematic) prior to study blood draw. Exclusion Criteria for Cancer Arm Participants: * Pregnancy or lactating women. * Recipients of organ transplant or prior non-autologous (allogeneic) bone marrow transplant or stem cell transplant. * Recipients of blood transfusion within 7 days prior to study blood draw. * Recipients of any anti-cancer therapy within 30 days prior to study blood draw, due to diseases other than cancers. * With other known malignant tumors or multiple primary tumors. Inclusion Criteria for Benign Arm Participants: * Age 40-75 years at the day of consenting to the study. * Able to provide a written informed consent. * Confirmed diagnosis of benign biliary tract diseases. * No prior radical treatment of the benign diseases prior to study blood draw. Exclusion Criteria for Benign Arm Participants: * Pregnancy or lactating women. * Recipients of organ transplant or prior non-autologous (allogeneic) bone marrow transplant or stem cell transplant. * Recipients of blood transfusion within 7 days prior to study blood draw. * Recipients of any anti-cancer therapy within 30 days prior to study blood draw, due to diseases other than cancers. * Confirmed diagnosis of malignancies or precancerous lesion. * A history of malignant tumors.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 40 Years
Maximum Age: 75 Years
Study: NCT05667350
Study Brief:
Protocol Section: NCT05667350