SYMPLIFY – assessing a multi-cancer early detection test in individuals referred with signs and symptoms of cancer
- Conditions
- Early detection of cancerCancer
- Registration Number
- ISRCTN10226380
- Lead Sponsor
- niversity of Oxford
- Brief Summary
2023 Results article in https://pubmed.ncbi.nlm.nih.gov/37352875/ (added 26/06/2023)
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 6238
1. Participants referred to an RDC or relevant 2WW pathway to rule a cancer diagnosis in or out will be invited to participate in the study.
2. Willing and able to give informed consent for participation in the study.
3. Male or Female, aged 18 years or above.
4. Referred to a RDC or a gynae, lung, upper GI or lower GI cancer 2WW pathway.
1. Has a history of invasive or haematological malignancy diagnosed within the previous 3 years.
2. Has undergone definitive treatment for invasive or haematological malignancy in the last 3 years (adjuvant hormone therapy is permissible in this context).
3. Is taking cytotoxic or demethylating agents such as methotrexate.
4. Previous or current participation in another GRAIL study. Participation” is defined as having signed consent and provided a blood sample.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method