A Single Dose Comfort Comparison of Travatan Z in One Eye Versus Xalatan in the Opposite Eye in Patients With Primary Open-Angle Glaucoma or Ocular Hypertension
Phase 4
Completed
- Conditions
- Open-Angle GlaucomaOcular Hypertension
- Interventions
- Registration Number
- NCT00527592
- Lead Sponsor
- Alcon Research
- Brief Summary
The purpose of this study is to compare the comfort of Travatan Z in one eye and Xalatan in the opposite eye in patients with primary open-angle glaucoma or ocular hypertension.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 54
Inclusion Criteria
- 18 years of age or older.
- Clinical diagnosis of ocular hypertension, primary open-angle, pigment dispersion, or exfoliation glaucoma in both eyes.
- Best corrected visual acuity of 20/200 Snellen or better in each eye.
- Intraocular pressure within protocol-specified range.
- Other protocol-defined inclusion criteria may apply.
Exclusion Criteria
- Any abnormality preventing reliable applanation tonometry in the study eye(s).
- Any eye conditions or procedures as specified in protocol.
- Progressive retinal or optic nerve disease from any cause.
- Use of contact lenses in the study eye(s).
- Other protocol-defined exclusion criteria may apply.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Travoprost Travoprost ophthalmic solution 0.004% with SofZia® preservative system (TRAVATAN Z®) Travoprost assigned to one eye, with latanoprost assigned to the fellow eye for intra-individual control. One drop, single dose. The eye, and the order in which the first test medicine was instilled (either travoprost or latanoprost), was randomly assigned. Latanoprost Latanoprost ophthalmic solution 0.005% (XALATAN®) Latanoprost assigned to one eye, with travoprost assigned to the fellow eye for intra-individual control. One drop, single dose. The eye, and the order in which the first test medicine was instilled (either travoprost or latanoprost), was randomly assigned.
- Primary Outcome Measures
Name Time Method Comfort Immediately After Dosing 5 seconds Comfort was assessed by the patient and recorded on a scale of 0 to 100, with 0 = perfect comfort and 100 = worse discomfort imaginable.
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
How do the preservatives in Travatan Z and Xalatan affect FP receptor activation and ocular surface integrity in glaucoma?
What is the comparative effectiveness of Travatan Z vs. Xalatan in IOP reduction and patient adherence in POAG?
Are there biomarkers that predict better ocular comfort with Travatan Z over Xalatan in patients with ocular hypertension?
What adverse events were reported in NCT00527592 and how do they compare to other prostaglandin analogs in Phase 4 trials?
How do newer preservative systems in prostaglandin analogs like Travatan Z influence comfort compared to traditional formulations?