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CompletedNCT00626847Updated Nov 21, 2016

How Does Your Genetic Make-up (Profile) Influence Your Glaucoma?

An observational study in Primary Open Angle Glaucoma, sponsored by Wills Eye. Completed at 1 site in United States. Open to participants aged 40 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-11-21.

Sponsored by Wills Eye · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
97
Ages
40 Years and older
Sex
All
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Study summary

Glaucoma is a group of diseases in which visual loss occurs because of damage to the optic nerve. Research has shown that certain genes may cause glaucoma in some cases. So far, research has only been able to find the genes responsible for glaucoma in a small percentage of people who have glaucoma. The purpose of this project is to study the genes in patients with and without glaucoma to find additional genes that may be responsible for causing glaucoma.

Read the detailed description

Four tubes of blood will be taken from 100 people. Of those, half will have primary open angle glaucoma (POAG) and the other half will be controls (normals), half will be caucasians and the other half will be african americans, half male and half female. All groups will have a routine ophthalmic eye exam, color vision, snellen vision, and visual field done.

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Conditions studied

  • Primary Open Angle Glaucoma

Keywords

  • primary open angle glaucoma
  • Nuclear Genetics
  • Mitochondrial DNA
  • POAG
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In context

Glaucoma

1,818 studies on the registry are indexed under Glaucoma; 231 are open to participants now.

This study's enrollment of 97 is close to the median of 103 across 454 observational studies indexed under Glaucoma.

Browse Glaucoma studies →

Lead sponsor

Wills Eye is the lead sponsor of 74 studies on the registry; 3 are open to participants now.

Of its 12 completed or terminated interventional studies of FDA-regulated products, 10 (83%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
40 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

glaucoma clinic

Inclusion criteria

  • 40 yrs
  • Caucasian or African American
  • Male or female with POAG, PACG, PXFG,
  • Normal

Exclusion criteria

Exclusion Criteria:

  • Other ophthamic co-morbidities
  • Other ethnic groups
  • Unable to understand and give informed consent
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
97 participants (actual)
Biospecimen retention
Samples with dna

Groups and cohorts

  • 1

    Primary Open Angle Glaucoma (POAG)

  • 2

    Controls (Normals, patients without glaucoma)

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What researchers measure

Primary outcomes

  1. The investigators will quantify the spectrum of changes in mitochondrial respiration, relative mitochondrial DNA content, and oxidative stress associated with different types of glaucoma.

    Time frame: one blood draw

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Study locations

1 site
  • Wills Eye Glaucoma Service
    Philadelphia, Pennsylvania 19107, United States
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References and documents

Publications

  • Abu-Amero KK, Azad TA, Spaeth GL, Myers J, Katz LJ, Moster M, Bosley TM. Unaltered myocilin expression in the blood of primary open angle glaucoma patients. Mol Vis. 2012;18:1004-9. Epub 2012 Apr 21. PubMed 22550394 ↗
  • Abu-Amero KK, Azad TA, Spaeth GL, Myers J, Katz LJ, Moster M, Bosley TM. Absence of altered expression of optineurin in primary open angle glaucoma patients. Mol Vis. 2012;18:1421-7. Epub 2012 Jun 1. PubMed 22690120 ↗

Individual participant data

Plan to share: Yes — Two manuscripts have been written and published.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 21, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00626847
Lead sponsor
Wills Eye
Collaborators
Jefferson Medical College of Thomas Jefferson University, Thomas Jefferson University
Responsible party
George L. Spaeth MD (Director Glaucoma Research Center Wills Eye; Director Medical Research and Education Glaucoma Service Foundation Wills Eye; Esposito Research Professor, Thomas Jefferson University, Wills Eye) — Principal investigator
First posted
Feb 29, 2008
Start date
Mar 2008
Primary completion
Aug 2009
Completion
Aug 2009
Last update
Nov 21, 2016

Study contacts

George L Spaeth, MD
principal investigator · Wills Eye Institute

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2016. You cannot join it, but the record below documents what was studied.

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