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NCT01931904Active, not recruiting

Eye Pressure Lowering Surgery

Observational Study of Ocular Blood Flow Pre- and Post- Glaucoma Surgery Using Functional and Structural Optical Coherence Tomography

Source: ClinicalTrials.gov · Last updated 2 Sept 2026

Brief summary (registry, in English)

The purpose of this study is to determine if lowering the pressure inside the eye improves blood flow to the eye.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
21 (estimated)
First submitted
27 Aug 2013
Start date
1 Feb 2014
Primary completion date
31 May 2031
Lead sponsor
Oregon Health and Science University
Diseases
Glaucoma
NCT number
NCT01931904

What you commit to

  • Study type: Observational
  • Planned participants: 21
  • From 1 Feb 2014 to the primary completion date, 31 May 2031
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous vision correction surgery such as Laser-Assisted in situ Keratomileusis (LASIK) or Photorefractive Keratectomy (PRK)
  • Previous intraocular surgery except for uncomplicated cataract extraction with posterior chamber intraocular lens implantation

Other illness

  • History of heart failure, myocardial infarction, transient ischemic attack or stroke
  • Other diseases that may cause VF loss or optic disc abnormalities
  • Life-threatening or debilitating illness making it unlikely patient will successfully complete the study.

Age

  • Age \< 18 or \>85 years

Other

  • Best-corrected visual acuity less than 20/40
  • Refractive error of \> +3.00 D or \< -7.00 D
  • Diabetic retinopathy
  • Inability to clinically view or photograph the optic discs due to media opacity or poorly dilating pupil
  • Inability to perform reliably on automated VF testing
  • Refusal of informed consent or of commitment to the full length of the study

Who the study is looking for

  • Subjects diagnosed with perimetric open angle glaucoma or chronic angle closure glaucoma.
  • Subjects scheduled to undergo trabeculectomy or tube shunt surgery

Age in the registry: 18 years to 85 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
OHSU
Coordinator of this site? Confirm its status
PortlandUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.