NCT04706481

Brief Summary

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

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
10,000

participants targeted

Target at P75+ for all trials

Timeline
299mo left

Started Jan 2020

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress21%
Jan 2020Dec 2050

Study Start

First participant enrolled

January 1, 2020

Completed
12 months until next milestone

First Submitted

Initial submission to the registry

December 28, 2020

Completed
15 days until next milestone

First Posted

Study publicly available on registry

January 12, 2021

Completed
29.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2050

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2050

Last Updated

March 12, 2026

Status Verified

March 1, 2026

Enrollment Period

30.9 years

First QC Date

December 28, 2020

Last Update Submit

March 11, 2026

Conditions

Keywords

Biobanking

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

Procedure: Specimen Collection

Cancer or Other Diseases

Diseased subjects who have provided consent for specimen collection

Procedure: Specimen Collection

Interventions

Specimens obtained from surgical, phlebotomy or other non-invasive procedure

Cancer or Other DiseasesHealthy Control

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

RECRUITING

Related Links

Biospecimen

Retention: SAMPLES WITH DNA

Buffy coats, plasma, serum, tissues, pleural effusion, urine and stool, etc

MeSH Terms

Conditions

NeoplasmsHeart DiseasesKidney DiseasesDiabetes MellitusDisease

Interventions

Specimen Handling

Condition Hierarchy (Ancestors)

Cardiovascular DiseasesUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesGlucose Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesEndocrine System DiseasesPathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Clinical Laboratory TechniquesDiagnostic Techniques and ProceduresDiagnosisInvestigative Techniques

Study Officials

  • Ching Wan MA, MB BChir

    Chinese University of Hong Kong

    STUDY CHAIR

Central Study Contacts

Terry OR, Ph.D

CONTACT

Marcus LAW, M. Phil

CONTACT

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

Locations