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DementiaNCT00878280

Copy Number Variations, Inflammatory Cytokines and the Risk of Dementia

An observational study of Dementia, run by National Taiwan University Hospital at 1 site in Taiwan.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Assess the association of copy number variation (CNV) and inflammatory cytokine with the risk of dementia. Read more about this study

Who is it for?
Ages 50 years and olderHealthy volunteers can take part
Conditions the study is for
Dementia
How many people
700 participants
Where
1 siteTaiwan
Study dates
Aug 2008to Jul 2011
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 50 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: hospital recruited dementia patients and controls

Who may be able to join

  • hospital recruited dementia patients and controls

Who cannot join

None listed.

Trial locations and contacts

1 site in 1 country.

Yen-Ching Chen, ScD contact

886-2-33668019

chenkaren@yahoo.com

Taiwan1 site, 1 recruiting
  • National Taiwan University Hospital

    Taipei, 100

    yen-ching chen, ScD, 3366-8019, chenkaren@yahoo.com

    Recruiting

Other trials in Taiwan

About this study

Official title: Copy Number Variations, Expression of Inflammatory Cytokines and the Risk of Dementia - A Two-stage Genome-wide Association Study

Assess the association of copy number variation (CNV) and inflammatory cytokine with the risk of dementia.

Read the detailed description

This is a hospital-based case-control study. We plan to assess the association of CNV and inflammatory cytokine with the risk of dementia. Hopefully to find some genetic biomarkers to identify the risk of dementia at an early stage.

Conditions
Dementia
Medical subject headings
Dementia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT00878280
Study groupRoleWhat they receive
11:control(healthy subjects)
22:case(dementia patients)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Dementia

    Measured: Aug 2008-July 2011

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Apr 2009 (estimated)
  2. Study startAug 2008
  3. Primary completionJul 2011 (estimated)
  4. Study completionJul 2011 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Prospective
Enrolment
700 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00878280
Sponsor's protocol ID
200712102R-1
Status last verified
Apr 2011
First submitted
31 Aug 2008
Last updated
22 Apr 2011
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Dementia, run by National Taiwan University Hospital at 1 site in Taiwan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 22 Apr 2011. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Yen-Ching Chen, ScD (886-2-33668019, chenkaren@yahoo.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Dementia (time frame: Aug 2008-July 2011). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Apr 2011.

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