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View Clinical Trial (Medical Research Study)
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Exploratory Study Comparing Signs and Symptoms in Patients With Ocular Hypertension or Glaucoma Using Xalatan R® or Travatan Z® - NCT00799682-11581 (Clinical Trial 255870)
Permalink: http://www.ClinicalConnection.com/exp/ExpandedPatientViewStudy255870.aspx
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| City: |
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Valley Stream |
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State:
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NY |
| Zip Code: |
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11581 |
| Conditions: |
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Dry Eye Disease |
| Purpose: |
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The purpose of this study is to determine if there is a difference in the ocular signs and
symptoms of subjects' eyes using Xalatan® 0.005% versus Travatan Z® 0.004% based on the
outcome of subject assessment and clinical assessment in patients with Ocular Hypertension
or Glaucoma with mild to moderate dry eye at baseline in accordance with the Oxford Grading
Scale.
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| Study summary: |
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| Criteria: |
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Inclusion Criteria:
- Male or Female 18 years of age or older
- Only patients who satisfy all informed consent requirements may be included in the
study
- Be likely to complete the entire course of study and comply with study drop regimen,
guidelines and visits
- Able to understand drop instructions and instill study drops
- Patients must be on monotherapy for Ocular Hypertension or Glaucoma and agree to a
washout period, as according to Appendix E
- Patient has Ocular Hypertension, chronic Open-Angle Glaucoma, chronic Angle-Closure
Glaucoma with patent iridotomy/iridectomy, Pseudo Exfoliate Glaucoma, or Pigmentary
Glaucoma in each eye at screening visit.
- Patients using systemic non-glaucoma medications known to lower IOP may be included,
if on stable dose >30 days prior to screening visit and agree to maintain the regimen
throughout the course of the study.
- Patients using non-prescription eye drops or prescription topical eye drops for dry
eye may be included, if on stable dose 30 days prior to screening visit and agree to
maintain the regimen throughout the course of the study.
- Patients who wear contact lenses with a maintained wearing pattern for the duration
of the study
- Best Corrected LogMar VA of ≤0.70 =(20/100 Snellen equivalent)
- Hyperemia Grading ≤2
- IOP ≤ 30 mmHg
- Shirmers 3mm - 9.75mm
- Tear break-up time (TBUT) 4 seconds - 9seconds
- Must meet the Biomicroscopic Criteria for both eyes as defined by the Oxford Grading
Scale
- Generally good and stable overall health
Exclusion Criteria:
- Females of childbearing potential (those who are not surgically sterilized or
defined as one-year post-menopausal) are excluded from participation in the study if
they meet any one of the following conditions:They are currently pregnant,They have a
positive result on the urine pregnancy test at the Screening Visit,They intend to
become pregnant during the study period,They are breast-feeding,or They are not using
highly effective birth control measures:
- Hormonal-oral, implanted, transdermal or injected contraceptives;
- Mechanical-spermicide in conjunction with a barrier such as a condom or diaphragm or
IUD Note: All females of childbearing potential must consent to a urine pregnancy
test at Screening. Females of childbearing potential are to be instructed to inform
the investigator if they become pregnant during the study. Should this occur, the
Investigator shall immediately contact the Sponsor. For non-sexually active females,
abstinence may be regarded as an adequate method of birth control; however, if the
patient becomes sexually active during the study, she must agree to use adequate
birth control methods as defined above for the remainder of the study.
- Patients who are currently on an investigational agent or discontinued within 30 days
prior to the Screening Visit
- Uncontrolled systemic disease
- Patients who have a known medical history of allergy or sensitivity to prostaglandin
drugs (topical and/or systemic)
- Patient with any history of refractive surgery
- History of ocular trauma within the past six months in either eye
- History of ocular infection or ocular inflammation within the past three months in
either eye
- History of clinically relevant or progressive retinal disease such as retinal
degeneration, diabetic retinopathy, or retinal detachment in either eye based on the
assessment of the Investigator
- History of any severe ocular pathology according to the Oxford Grading Scale
- greater than Grade 4 dry eye) in either eye
- Intraocular surgery within the past six months as determined by patient history
and/or examination in either eye.
- Ocular laser surgery or Punctal Cautery within the past three months as determined by
patient history and/or examination in either eye
- Punctal Plugs insertion ≤ 7 days prior to (Visit 1) Screening
- Any abnormality preventing reliable applanation tonometry of either eye.
- Contraindication to pupil dilation or patients with cycloplegia
- Patients with best-corrected visual acuity score worse than 0.70 LogMar (20/100)
score in either eye
- Patients with ≤30 days stable dosing regimen before the Screening Visit of any
medications or substances administered by any route and used on a chronic basis
- History of Stevens-Johnson Syndrome or Ocular Pemphigoid
- History of liver disease
- Severe clinical vitamin deficiencies or history of vitamin overdose
- Highly variable self-administration of over-the-counter vitamin/herbal products
- Any steroid use within the past 30 days
- Corneal pathology, which could, and of itself, cause an ocular surface disorder
- Visual Field loss which in the opinion of the Investigator is functionally
significant or evidence of progress visual field loss within the last year prior to
the (Visit 2) Baseline/Randomization
- Patient has a condition or is in a situation which, in the investigator's opinion,
may put the subject at a significant risk, may confound study results, or may
interfere significantly with the subject's participation in the study. |
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| Study is available at: |
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Ophthalmic Consultants of Long Island
Valley Stream, NY 11581
United States
Primary Contact:
Julissa Diaz
Email: jdiaz@ocli.net
Phone: 516-593-4026
Secondary Contact:
Julissa Diaz
Email: jdiaz@ocli.net
Phone: (516) 593-4026 |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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March 16, 2010 |
Modifications to
this listing: |
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Only selected fields are shown, please use the link
above to view all information about this clinical trial. |
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Clinical trials are medical research studies designed to test the safety and/or
effectiveness of new drugs, devices, or treatments in humans. These studies are
conducted worldwide for a range of conditions and illnesses. Learn more about
clinical research and participating in a study at
About Clinical Trials.
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