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Characterization of Potential Biomarkers of Eye Disease and Vision (EYE-MARKER)

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ClinicalTrials.gov Identifier: NCT02500862
Recruitment Status : Active, not recruiting
First Posted : July 17, 2015
Last Update Posted : January 15, 2019
Sponsor:
Information provided by (Responsible Party):
Association for Innovation and Biomedical Research on Light and Image

Brief Summary:
Characterize potential biomarkers of sight-threatening eye diseases based on the information acquired in clinical practice at CEC, AIBILI

Condition or disease
Eye Disease

Detailed Description:

This is a registry study. Only patients followed under the clinical practice at AIBILI Clinical Trial Centre, and with a signed informed consent form will be included.

Based on the clinical information collected under the clinical practice, and based on patients' characteristics, scientific questions will be raised and data will be collected and analysed accordingly.

Any procedure performed under clinical practice that may allow for the characterization of the disease and/or for the identification of potential biomarkers will be collected and analysed.


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Study Type : Observational [Patient Registry]
Estimated Enrollment : 100 participants
Observational Model: Other
Time Perspective: Other
Target Follow-Up Duration: 10 Years
Official Title: Characterization of Potential Biomarkers of Eye Disease and Vision Loss.
Study Start Date : September 2015
Estimated Primary Completion Date : December 2019
Estimated Study Completion Date : December 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Eye Diseases




Primary Outcome Measures :
  1. Characterize potential biomarkers of sight-threatening eye diseases based on the information acquired in clinical practice at CEC, AIBILI. [ Time Frame: 10 years ]


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
Any patient followed under the normal clinical practice at AIBILI Clinical Trial Centre, and with a AIBILI signed informed consent form for data collection, Imp. 11-7-2 "Consentimento Informado para tratamento de dados".
Criteria

Inclusion Criteria:

  • Any patient followed under the normal clinical practice at AIBILI Clinical Trial Centre, and with a AIBILI signed informed consent form for data collection, Imp. 11-7-2 "Consentimento Informado para tratamento de dados".

Exclusion criteria:

  • None

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02500862


Locations
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Portugal
CEC
Coimbra, Portugal, 3000-548
Sponsors and Collaborators
Association for Innovation and Biomedical Research on Light and Image
Investigators
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Principal Investigator: Maria L Ribeiro, MsC Association for Innovation and Biomedical Research on Light and Image

Additional Information:

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Responsible Party: Association for Innovation and Biomedical Research on Light and Image
ClinicalTrials.gov Identifier: NCT02500862     History of Changes
Other Study ID Numbers: 4C-2015-08
First Posted: July 17, 2015    Key Record Dates
Last Update Posted: January 15, 2019
Last Verified: January 2019

Keywords provided by Association for Innovation and Biomedical Research on Light and Image:
Eye
Imaging

Additional relevant MeSH terms:
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Eye Diseases