Collection and storage of human biological samples for research
Archival of Human Biological Samples in CU-Med Biobank
Chinese University of Hong Kong · NCT04706481
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 |
|---|---|
| Enrollment | 10000 (estimated) |
| Sex | All |
| Sponsor | Chinese University of Hong Kong (other) |
| Locations | 1 site (Hong Kong) |
| Trial ID | NCT04706481 on ClinicalTrials.gov |
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.
Who should consider this trial
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.
Not a fit: Patients who do not wish to provide informed consent for their biological samples and data will not benefit from this biobank.
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 performed: Other biobanking initiatives have shown success in supporting research and improving patient outcomes, indicating that this approach is well-established.
Eligibility criteria
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 this trial is running
Hong Kong
- CU-Med Biobank — Hong Kong, Hong Kong (RECRUITING)
Study contacts
- Study coordinator: Terry OR, Ph.D
- Email: terryor@cuhk.edu.hk
- Phone: 852-26285221
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Healthy, Cancer, Heart Diseases, Neurological Diseases or Conditions, Kidney Diseases, Diabetes, Other Disease, Biobanking