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Collection of Blood Specimens From Patients in AL-3789 Studies for Elevated Intraocular Pressure (IOP)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00691639
First Posted: June 5, 2008
Last Update Posted: October 1, 2009
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Alcon Research
  Purpose
The objective of this study is to obtain blood samples from patients who are or were participants in any Alcon AL-3789 clinical trial. Association will be conducted to search for genetic markers in patients with glaucoma or ocular hypertension.

Condition Intervention
Open-Angle Glaucoma Other: Blood Collection Only

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Retrospective
Official Title: Collection of Blood Specimens From Patients in AL-3789 Studies for Elevated Intraocular Pressure (IOP)

Resource links provided by NLM:


Further study details as provided by Alcon Research:

Estimated Enrollment: 1000
Study Start Date: March 2008
Primary Completion Date: August 2009 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
1
Patients who are or were participants in any Alcon AL-3789 study.
Other: Blood Collection Only
Blood Collection Only

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Patients who received anecortave acetate treatment
Criteria

Inclusion Criteria:

  • Patient must be currently or previously enrolled in Alcon clinical study and received AL-3789

Exclusion Criteria:

  • Age related
  Contacts and Locations
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): NCT00691639


Locations
United States, Texas
Alcon Call Center
Fort Worth, Texas, United States, 76134
Sponsors and Collaborators
Alcon Research
  More Information

Responsible Party: Alberta Davis, Alcon
ClinicalTrials.gov Identifier: NCT00691639     History of Changes
Other Study ID Numbers: C-07-27
First Submitted: June 3, 2008
First Posted: June 5, 2008
Last Update Posted: October 1, 2009
Last Verified: September 2009

Keywords provided by Alcon Research:
Open-angle glaucoma
IOP

Additional relevant MeSH terms:
Glaucoma
Glaucoma, Open-Angle
Ocular Hypertension
Eye Diseases