TCTR20130325001CompletedPhase 3
A randomized comparative study of the efficacy on pupillary dilatation between separate bottles of dilating eye drops and a single-bottle eye drop mixture.
Conditions
Trial Snapshot
- Phase
- Phase 3
- Status
- Completed
- Sponsor
- one
- Enrollment
- 28
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 Years to 0 N/A (No limit) (—)
- Sex
- All
Inclusion Criteria
- •- age 18 or older
- •- clear cornea (pupil can be easily measured)
- •- patients with hypertension must have resting BP not more than 160/95 mmHg
- •- patient receives studied eye drops in only 1 eye
Exclusion Criteria
- •- pupil distortion or any congenital anomaly of pupil (such as corectopia)
- •- untreated appositional angle or angle closure
- •- pregnancy
- •- allergic to any of the study drugs
- •- patient who cannot complete the study
Investigators
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