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Ocular Blood Flow in Early Glaucoma Patients Before and After Treatment With Dorzolamide

Primary Purpose

Glaucoma

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Dorzolamide 2% drops
HRF and CLBF
Sponsored by
University Health Network, Toronto
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Glaucoma focused on measuring Glaucoma, Intraocular pressure, Ocular blood flow, Laser-Doppler Flowmetry

Eligibility Criteria

20 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Males or females 20-80 years of age. Presence of typical early glaucomatous optic disc changes (cup/disc ratio ≤ 0.75) and/or early glaucomatous visual field defects (mean deviation less than 5dB and outside of 10° from fixation) in the study eye at the baseline visit. Best corrected visual acuity of at least 20/40. Signed informed consent from the subject The subject should be able to understand the instructions and perform the HRF and CLBF tests as well as be willing and able to comply with the study schedule and treatment. Exclusion Criteria: Pregnant women or nursing mothers. Any other active ocular disease (ocular infections, Uveitis, etc.) Known allergy or sensitivity to the study medications. Functionally significant visual field loss (mean deviation greater than 5dB) or cup/disc ratio greater than 0.75 or evidence of progressive visual field loss within the last 6 months. Required chronic use of other ocular or systemic hypotensive medications during the study, other than the study medication (e.g. beta-blockers, Ca-channel blockers) Vascular occlusive disease affecting the ocular circulation such as: diabetic retinopathy, central retinal vein occlusion, central retinal artery occlusion, or non-arteritic ischemic optic neuropathy. Previous intraocular surgery or ocular traumas. Any past history of serious systemic condition affecting cerebral circulation including: hypertension, diabetes, cerebral vascular accident (CVA), or coronary artery bypass graft (CABG).

Sites / Locations

  • Department of Ophthalmology and Visual Sciences; Toronto Western HospitalRecruiting

Outcomes

Primary Outcome Measures

Ocular blood flow measurements

Secondary Outcome Measures

Intraocular pressure reduction

Full Information

First Posted
September 8, 2005
Last Updated
July 23, 2007
Sponsor
University Health Network, Toronto
Collaborators
Merck Frosst Canada Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT00152932
Brief Title
Ocular Blood Flow in Early Glaucoma Patients Before and After Treatment With Dorzolamide
Official Title
Ocular Blood Flow Measured by HRF and CLBF in Newly Diagnosed and Early Glaucoma Patients Before and After Instillation of Dorzolamide 2%
Study Type
Interventional

2. Study Status

Record Verification Date
September 2005
Overall Recruitment Status
Unknown status
Study Start Date
May 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
June 2006 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
University Health Network, Toronto
Collaborators
Merck Frosst Canada Ltd.

4. Oversight

5. Study Description

Brief Summary
Impaired ocular blood flow is an important risk factor in the pathogenesis of primary open angle glaucoma (POAG). A few studies suggest that topical dorzolamide 2% may increase optic nerve perfusion. The objectives of this study are to learn the effects of dorzolamide on the retinal and optic nerve blood flow of glaucoma patients. The present study is a prospective, randomized, double-masked, crossover design study of newly diagnosed or already treated patients with early glaucoma. The investigators will check ocular blood flow parameters using the Canon Laser Blood Flowmeter (CLBF), used to evaluate retinal arteriole blood flow, and the Heidelberg retinal flowmeter (HRF), which measures blood flow through capillary beds in the retina and optic nerve head. Any demonstrated improvements to retinal and optic nerve blood flow with dorzolamide, will mean that the drug may protect against ischaemic nerve and retinal damage. Any documented improvement in flow could lead to a major change in the management of glaucoma patients as well as other retinal ischemic diseases such as diabetic retinopathy and central retinal vein occlusion.
Detailed Description
High intraocular pressure (IOP) is the major risk factor for glaucoma. Lowering intraocular pressure is still the only accepted form of treatment for glaucoma. Over the past decade, epidemiological and experimental evidence suggested that impaired ocular blood flow is an important risk factor with an important role in the pathogenesis of primary open angle glaucoma (POAG). Several studies suggest that ischemia-promoting vascular factors may contribute to glaucomatous damage including vasospasm, impaired ocular perfusion pressure and general vascular disorders such as low blood pressure, especially dips in blood pressure at night. Different techniques are employed to assess vascular dysfunction in the eye. As the methodology of ocular blood flow assessment is complex and differs in various aspects (e.g. target tissue and physiological parameters), comparative studies are required in order to enhance the interpretation of these measurements. Our laboratory has state of the art equipment to assess ocular blood flow. One study done by us suggested that one drop of Dorzolamide 2% does not improve retinal blood flow in normal eyes. In the present study we plan to extend this study to 2 weeks of treatment in patients with POAG. Dorzolamide hydrochloride 2% is a topical carbonic anhydrase inhibitor which reduces intraocular pressure (IOP) by decreasing the production of aqueous humour. Pharmacological studies on volunteers and glaucoma patients, using Color Doppler Imaging (measuring the retrobulbar blood flow) and Scanning laser Ophthalmoscopy (measuring arteriovenous passage time), indicate that topically applied Dorzolamide may increase perfusion of the optic nerve and peripapillary retina.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glaucoma
Keywords
Glaucoma, Intraocular pressure, Ocular blood flow, Laser-Doppler Flowmetry

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Single
Allocation
Randomized
Enrollment
17 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Dorzolamide 2% drops
Intervention Type
Device
Intervention Name(s)
HRF and CLBF
Primary Outcome Measure Information:
Title
Ocular blood flow measurements
Secondary Outcome Measure Information:
Title
Intraocular pressure reduction

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Males or females 20-80 years of age. Presence of typical early glaucomatous optic disc changes (cup/disc ratio ≤ 0.75) and/or early glaucomatous visual field defects (mean deviation less than 5dB and outside of 10° from fixation) in the study eye at the baseline visit. Best corrected visual acuity of at least 20/40. Signed informed consent from the subject The subject should be able to understand the instructions and perform the HRF and CLBF tests as well as be willing and able to comply with the study schedule and treatment. Exclusion Criteria: Pregnant women or nursing mothers. Any other active ocular disease (ocular infections, Uveitis, etc.) Known allergy or sensitivity to the study medications. Functionally significant visual field loss (mean deviation greater than 5dB) or cup/disc ratio greater than 0.75 or evidence of progressive visual field loss within the last 6 months. Required chronic use of other ocular or systemic hypotensive medications during the study, other than the study medication (e.g. beta-blockers, Ca-channel blockers) Vascular occlusive disease affecting the ocular circulation such as: diabetic retinopathy, central retinal vein occlusion, central retinal artery occlusion, or non-arteritic ischemic optic neuropathy. Previous intraocular surgery or ocular traumas. Any past history of serious systemic condition affecting cerebral circulation including: hypertension, diabetes, cerebral vascular accident (CVA), or coronary artery bypass graft (CABG).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rony Rachmiel, MD
Phone
416-603-5317
Email
rachmiel_r@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Graham E Trope, MB, FRCSC
Organizational Affiliation
University of Toronto, Department of Ophthalmology
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Chris Hudson, PhD
Organizational Affiliation
Department of Ophthalmology, Toronto Western Hospital, Toronto
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
John Flanagan, PhD
Organizational Affiliation
Department of Ophthalmology, Toronto Western Hospital, Toronto
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Yvonne M Buys, MD, FRCSC
Organizational Affiliation
University of Toronto, Department of Ophthalmology, Toronto Western Hospital, Toronto
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Ophthalmology and Visual Sciences; Toronto Western Hospital
City
Toronto
State/Province
Ontario
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rony Rachmiel, MD
Phone
416-603-5317
Email
rachmiel_r@hotmail.com
First Name & Middle Initial & Last Name & Degree
Graham E Trope, MB PhD, FRCSC
Phone
416-603-5317
Email
Graham.Trope@uhn.on.ca
First Name & Middle Initial & Last Name & Degree
Rony Rachmiel, MD

12. IPD Sharing Statement

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Ocular Blood Flow in Early Glaucoma Patients Before and After Treatment With Dorzolamide

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