- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00465348
The Antioxidant Effect of Routine Vascular Therapy for Normal Tension Glaucoma Patients
Study Overview
Status
Conditions
Detailed Description
There are two accepted medical modalities for glaucoma treatment. The first, is a local application of an intraocular pressure (IOP) lowering drug. The second, is the application of systemic drugs to improve vascular regulation. In the present study we would like to investigate whether this systemic form of treatment, in addition to improving blood flow, also reduces systemic oxidative stress.
Vascular dysregulation is one of the major risk factors for glaucoma, in particular for normal tension glaucoma (NTG). In glaucoma patients blood flow is, on average, reduced not only in the eye but also in various other organs of the body, for example in the fingers. Such a systemic dysregulation leads to disturbed autoregulation and thereby to an unstable oxygen supply in the eye.This, in turn, leads to the formation of reactive oxygen species (ROS). These ROS are capable of damaging cells such as white blood cells; this damage, however, is reversible as nature has provided us with mechanisms to repair this damage. This reversible damage brought about by ROS, which is constantly being repaired in our body, is an indication for oxidative stress. Oxidative stress plays an important role in the pathogenesis of glaucoma.
The indications for oxidative stress can be quantified in our laboratory by the method of comet assay also known as single cell gel electrophoresis.
Study Type
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
For NTG patients:
- A mean untreated intraocular pressure consistently equal to or below 21mmHg or median intraocular pressure equal to or below 20mmHg on diurnal testing (at least three measurements) with no single measurement greater than 24mmHg
- Open drainage angles on gonioscopy
- Typical optic disc damage with glaucomatous cupping and thinning of neuroretinal rim
- Visual field defect congruent to glaucomatous disc alteration
- No other pathological findings upon slit-lamp examination and indirect fundoscopy
- Vasospastic propensity will be assumed if a clear history of frequent cold hands (answering yes to the questions:" Do you always have cold hands, even during the summer time?" and "Do other people tell you that you have cold hands?") is reported.
For healthy subjects:
- An intraocular pressure < 20 mmHg
- No history of ocular or systemic disease
- No history of chronic or current systemic or topical medication, or of drug or alcohol abuse
- Normal blood pressure (100-140/60-90mm Hg)
- Best corrected visual acuity above 20/32 in both eyes
- No pathological findings upon slit-lamp examination and indirect fundoscopy
Exclusion Criteria:
EXCLUSION CRITERIA:
- Iridocorneal angle extremely narrow with complete or partial closure as determined by gonioscopy
- Pigmentary dispersion or pseudoexfoliation
- Evidence for any secondary cause for a glaucomatous optic neuropathy (trauma, steroids, uveitis)
- History of chronic or recurrent severe inflammatory eye disease (eg. scleritis, uveitis) or clinically significant or progressive retinal disease (eg. diabetic retinopathy)
- History of ocular trauma or intraocular surgery within the past 6 months
- History of systemic infection or inflammation within the past 3 months
- Need for any concomitant medications that may interfere with the evaluation of leukocytes (eg: steroids, immunosuppressives)
- Patients with a significant history and /or active alcohol or drug abuse (significant is defined as that which may influence results of the study)
Study Plan
How is the study designed?
Design Details
Collaborators and Investigators
Investigators
- Study Director: Selim Orgül, MD, University Hospital Basel, Eye Clinic
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 085-Mom-2007
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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