ProSight: a Multi-centre Interventional Study Evaluating MCED in Asymptomatic Population (NCT06790355) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
ProSight: a Multi-centre Interventional Study Evaluating MCED in Asymptomatic Population
2,527 participantsStarted 2025-03-01
Plain-language summary
This is a prospective, multi-centre interventional study evaluating the feasibility of blood-based multi-cancer early detection test in asymptomatic screening cohort.
Who can participate
Age range40 Years – 74 Years
SexALL
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Inclusion Criteria:
* 40-74 years old
* Able to provide a written informed consent and willing to comply with all parts of the protocol procedures
Exclusion Criteria:
* With cancer-associated clinical symptoms or suspected of cancer within 30 days prior to screen
* Have definite contraindications of cancer screening examination and diagnostic procedures
* Unable to comply with the protocol procedures
* Personal history of cancer, diagnosed within the 3 years prior to expected enrollment date
* Have received or are undergoing curative cancer treatment within three years prior to recruitment. Adjuvant endocrinotherapy for cancer is not an exclusion criterion.
* Recipients of anti-tumor therapy within 30 days prior to screen
* Pregnancy or lactating women
* Recipients of organ transplant or prior bone marrow transplant or stem cell transplant
* Recipients of blood transfusion within 7 days prior to screen
* With autoimmune diseases
* Have an acute infection or inflammation or uncontrolled chronic infection within 14 days prior to blood draw
* Unsuitable for this trial determined by the researchers (eg. hemorrhagic diseases)
What they're measuring
1
Feasibility of MCED in the intended use setting.
Timeframe: From enrollment to the Follow-up at 1 year
2
Safety of MCED in the intended use setting.
Timeframe: From enrollment to the Follow-up at 1 year
Trial details
NCT IDNCT06790355
SponsorShanghai Weihe Medical Laboratory Co., Ltd.