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NCT01240343 Clinical Trial

Creation of the Biobank Related to Eye Disease

Eye Diseases Clinical Trial

— BioBank  

Official title:
Creation of the Biobank Related to Eye Disease

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01240343
Other study ID # 2009-057
Secondary ID
Status Completed
Phase N/A
First received November 10, 2010
Last updated January 10, 2018
Start date June 2009
Est. completion date December 4, 2017

Study information
Verified date January 2018
Source William Beaumont Hospitals
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to develop a BioBank (a specialized lab) and collect blood, fluids and/or other tissue samples to study eye diseases.

Description:

The purpose of the Biobank related to eye disease at Beaumont Hospital is to help connect specialties and Specialists with each other, outside traditional limits of hospital or laboratory departments. The specimens (blood, fluids, and/or tissue samples) that will be collected from men, women and children will assist the researchers in a variety of studies on human eye diseases.

Research utilizing these specimens will allow for an increased understanding of the etiology, disease process, and response to treatments for various eye diseases, and will provide opportunities to subsequently improve our management decisions. Furthermore, projects that cross over between subspecialties are sparse and that is a limiting factor for the development of research that takes a more comprehensive approach.

Recruitment information / eligibility
Status Completed
Enrollment 669
Est. completion date December 4, 2017
Est. primary completion date December 4, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: All pediatric and adult patients age 0-99 years -

Exclusion Criteria: All patients who do not agree to consent for collection of blood, fluids, tissue.

Patients who are cognitively impaired and are not able to verbalize understanding of the risks/benefits.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States William Beaumont Hospital Royal Oak Michigan

Sponsors (2)
Lead Sponsor Collaborator
Kimberly Drenser Vision Research Foundation

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary To build the platform for a novel application of translational research that links cutting edge molecular laboratory techniques to clinical outcome studies Biobanks can be used for numberous discovery applications such as: identification and structural characterization of human genes, expression analysis, or discovery proteomics. Biological specimens, when coupled with standardized treatment and outcome data, will be essential resources for the identification, characterization and validation of biomarkers that are predictive of disease and treatment.
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