About this trial

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

Eligibility criteria

Qualifiers

Enrolled subjects that have provided signed consent for the specimens and de-identified data to be collected, stored and distributed.

Disqualifiers

Subjects without signed informed consent for the specimens and de-identified data to be collected, stored and distributed.

Trial design

Treatments tested in this trial

  • Specimen Collection

Treatment groups

10,000 Participants
are divided into 2 treatment groups

Locations

1
CU-Med Biobank Hong Kong Hong Kong

Sponsors and collaborators

Chinese University of Hong Kong

Lead sponsor