Archival of Human Biological Samples in CU-Med Biobank
1 other identifier
observational
10,000
1 country
1
Brief Summary
CU-Med Biobank collaborates with different researchers for collecting and distributing human biospecimens and clinical data for assisting scientific research.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2020
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2020
CompletedFirst Submitted
Initial submission to the registry
December 28, 2020
CompletedFirst Posted
Study publicly available on registry
January 12, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2050
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2050
March 12, 2026
March 1, 2026
30.9 years
December 28, 2020
March 11, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
To distribute human biospecimens for clinical research
By using the biological samples from CU-Med Biobank, translational studies can be done.
99 years
To discover the pathological mechanism of different acute and chronic diseases such as cancer, stroke, heart disease, dementia & diabetes
The relationship between different genome/proteome/bacteriome/virome and various diseases can be revealed, thus leading to a better prognostic and diagnostic outcome.
99 years
Study Arms (2)
Healthy Control
Healthy subjects who have provided consent for specimen collection
Cancer or Other Diseases
Diseased subjects who have provided consent for specimen collection
Interventions
Specimens obtained from surgical, phlebotomy or other non-invasive procedure
Eligibility Criteria
The diverse group of biorepositories with focus on normal cohorts and cancer-related or other disease cohorts.
You may qualify if:
- Enrolled subjects that have provided signed consent for the specimens and de-identified data to be collected, stored and distributed.
You may not qualify if:
- Subjects without signed informed consent for the specimens and de-identified data to be collected, stored and distributed.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CU-Med Biobank
Hong Kong, Hong Kong
Related Links
Biospecimen
Buffy coats, plasma, serum, tissues, pleural effusion, urine and stool, etc
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Ching Wan MA, MB BChir
Chinese University of Hong Kong
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 99 Years
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
December 28, 2020
First Posted
January 12, 2021
Study Start
January 1, 2020
Primary Completion (Estimated)
December 1, 2050
Study Completion (Estimated)
December 1, 2050
Last Updated
March 12, 2026
Record last verified: 2026-03