NCT03291392

Brief Summary

The purpose of the study are:

  1. 1.To make quality, characterized samples and related data available for future studies, including Genome Wide Association Studies (GWAS), genomics, and biomarker research;
  2. 2.To use these samples and related medical information to answer research questions aimed at understanding the genetics and underlying biology of acquired disease and injury to the brain, heart and blood vessels with the express purpose of advancing the search for effective modalities for prevention, treatment, and recovery;
  3. 3.To develop additional operational infrastructure to support this project across the Prince of Wales Hospital and divisions, including (1) tracking of patient consent, (2) management of collection and sample processing processes, (3) sample inventory and QC/QA processes, and (4) release of materials to investigators for further research.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
500

participants targeted

Target at P75+ for all trials

Timeline
20mo left

Started Jun 2015

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 Progress87%
Jun 2015Dec 2027

Study Start

First participant enrolled

June 15, 2015

Completed
2.3 years until next milestone

First Submitted

Initial submission to the registry

September 19, 2017

Completed
6 days until next milestone

First Posted

Study publicly available on registry

September 25, 2017

Completed
9.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2026

Expected
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2027

Last Updated

February 24, 2026

Status Verified

February 1, 2026

Enrollment Period

11.6 years

First QC Date

September 19, 2017

Last Update Submit

February 21, 2026

Conditions

Keywords

GeneticsStrokeBiobankAtherosclerosis

Outcome Measures

Primary Outcomes (1)

  • Ischemic stroke-related genetics

    1. Discovery of novel genetic predictor of stroke and its complications will be done by identifying cases and controls for different stroke subtype and complications within the recruited samples, and using whole-genome genotyping arrays, or by sequencing approaches. 2. Replication of novel genetic markers of stroke will be performed using a combination of genotyping, multiplex genotyping, customized-content genotyping arrays and sequencing.

    Dec, 2025

Study Arms (3)

Atherosclerosis

Patient with intracranial stenosis or extracranial stenosis equal to or more than 70% would be invited to join the study for blood taking. Biobank: Gene expression or biomarkers exploration for atherosclerotic-related genetic diseases

Genetic: Gene expression or biomarkers exploration

Family members

The stroke patient who had family history of stroke, their parents and siblings would also be invited to join the study for blood taking or buccal swab/ saliva collection. Biobank: Gene expression or biomarkers exploration for atherosclerotic-related genetic diseases

Genetic: Gene expression or biomarkers exploration

Normal subjects

Normal subjects without ischemic stroke or intracranial/extracranial stenosis would be invited to join the study for blood taking. Biobank: Gene expression or biomarkers exploration for atherosclerotic-related genetic diseases

Genetic: Gene expression or biomarkers exploration

Interventions

AtherosclerosisFamily membersNormal subjects

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

1. Chinese ONLY 2. Patients with intracranial stenosis or extracranial stenosis equal to or \>70% 3. Stroke patients and their family members 4. Normal subject without any intracranial stenosis/ extracranial stenosis

You may qualify if:

  • Adult equal or more 18 years of age and Chinese ONLY.
  • Stroke patients, their family members, and/or the normal subjects without intracranial stenosis or extracranial stenosis, are eligible to join the study.
  • Subject is willing to have blood taken, cerebral spinal fluid and/or body tissue drawn for storage in the research bank.

You may not qualify if:

  • None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Chinese University of Hong Kong

Hong Kong, Hong Kong

RECRUITING

Biospecimen

Retention: SAMPLES WITH DNA

30ml of EDTA blood, buccal swab or saliva, body tissue, or cerebrospinal fluid to be collected

MeSH Terms

Conditions

Ischemic StrokeGenetic Diseases, InbornIntracranial ArteriosclerosisStrokeAtherosclerosis

Interventions

Gene Expression

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular DiseasesCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesIntracranial Arterial DiseasesArteriosclerosisArterial Occlusive Diseases

Intervention Hierarchy (Ancestors)

Genetic Phenomena

Study Officials

  • Thomas Wai Hong LEUNG, FRCP

    Chinese University of Hong Kong

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Thomas Wai Hong LEUNG, FRCP

CONTACT

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

September 19, 2017

First Posted

September 25, 2017

Study Start

June 15, 2015

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2027

Last Updated

February 24, 2026

Record last verified: 2026-02

Locations