Collection and storage of human biological samples for research
Official title: Archival of Human Biological Samples in CU-Med Biobank
Run by Chinese University of Hong Kong · NCT04706481 · Data updated 2026-11-12
This study is about collecting and storing biological samples from people with different health conditions to help researchers find better ways to prevent, diagnose, and treat diseases.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 10000 (estimated) |
| Sponsor | Chinese University of Hong Kong Academic / other |
| Locations | 1 site (Hong Kong) |
| Status | Recruiting |
| Started | January 1, 2020 |
| Main results expected | December 1, 2050 |
| Study ends | December 1, 2050 |
| Registry record updated | March 12, 2026 |
| Trial ID | NCT04706481 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this biobank are individuals who are willing to provide informed consent for the collection and storage of their biological samples and clinical data.
✕Probably not a fit
Patients who do not wish to provide informed consent for their biological samples and data will not benefit from this biobank.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
CU-Med Biobank is focused on collecting and storing high-quality biological specimens from individuals with various health conditions, including cancer and heart diseases. The biobank links these samples to detailed clinical data obtained from participants who have provided informed consent. This initiative aims to support scientific research by providing researchers with essential biological materials and comprehensive clinical information. The standardized approach of CU-Med Biobank is designed to facilitate the translation of basic research into clinical applications, ultimately improving disease prevention, diagnosis, and treatment.
Why it matters
Potential benefit: If successful, this biobank could significantly enhance research capabilities, leading to better prevention strategies, improved diagnoses, and new treatments for various diseases.
How similar studies have gone: Other biobanking initiatives have shown success in supporting research and improving patient outcomes, indicating that this approach is well-established.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Enrolled subjects that have provided signed consent for the specimens and de-identified data to be collected, stored and distributed. Exclusion Criteria: * Subjects without signed informed consent for the specimens and de-identified data to be collected, stored and distributed.
Where it's running
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CU-Med Biobank
Hong Kong, Hong Kong Recruiting
Study contacts
- Study coordinator: Terry OR, Ph.D
- Email: terryor@cuhk.edu.hk
- Phone: 852-26285221
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.