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NCT04706481 Clinical Trial

Archival of Human Biological Samples in CU-Med Biobank

Healthy Clinical Trial

Official title:
Archival of Human Biological Samples in CU-Med Biobank

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04706481
Other study ID # CREC 2019.152
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2020
Est. completion date December 1, 2050

Study information
Verified date February 2024
Source Chinese University of Hong Kong
Contact Terry OR, Ph.D
Phone 852-26285221
Email terryor@cuhk.edu.hk
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

CU-Med Biobank collaborates with different researchers for collecting and distributing human biospecimens and clinical data for assisting scientific research.

Description:

CU-Med Biobank will collect and store high-quality specimens from cancer-related or other diseases. All samples are linked to annotated clinical data from approved consented protocols. This system provides researchers with high- quality biological samples and comprehensive clinical, pathological including molecular/genetic information for their research. This standardized CU-Med Biobank is a pivotal bridge to improve the translation of basic research into clinical applications. These findings will contribute to improve prevention, enhance diagnosis, develop new treatment and eventual cure of diseases.

Recruitment information / eligibility
Status Recruiting
Enrollment 10000
Est. completion date December 1, 2050
Est. primary completion date December 1, 2050
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility 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.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Specimen Collection
Specimens obtained from surgical, phlebotomy or other non-invasive procedure

Locations
Country Name City State
Hong Kong CU-Med Biobank Hong Kong

Sponsors (1)
Lead Sponsor Collaborator
Chinese University of Hong Kong

Country where clinical trial is conducted

Hong Kong, 

Outcome
Type Measure Description Time frame Safety issue
Primary To distribute human biospecimens for clinical research By using the biological samples from CU-Med Biobank, translational studies can be done. 99 years
Primary 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
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