Colorectal Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have been diagnosed with colorectal cancer (cancer of the colon or rectum), confirmed through laboratory testing of tissue, at any stage of the disease
- People aged 18 years or older
- People who are willing and able to sign a consent form agreeing to take part
- People who have tissue and blood samples already stored at the institution's biological sample bank (biobank) that can be used for research
Who may not be able to join:
- People where the process of collecting and storing tumour samples for the biobank could interfere with the tests needed to diagnose or assess their cancer
- People who are currently pregnant or breastfeeding
- People who have had another type of cancer in the past 5 years — though exceptions may apply for certain skin cancers that were adequately treated, or early-stage cervical cancer that was fully removed by surgery (confirm with trial site)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Vincenzo Canzonieri, MD,PhD, Centro di Riferimento Oncologico di Aviano (CRO) - IRCCS
Phone: 0434 659 618
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Frequency of overexpression of STARD3 in both early and advanced CRC patients
Can't join this trial?
Data last synced from ClinicalTrials.gov: 14 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.