Efficacy of PEG-400 and Systane Artificial Tears (Alcon) on Quality of Vision
Completed · Phase 4
Conditions studied: Myopia
In brief
To evaluate the effect of PEG-400 and Systane on quality of vision after LASIK.
Key facts
- Study ID
- NCT00627302
- Run by
- Bp Consulting, Inc
- People needed
- 40
- Starts
- 2008-02-01
- Expected to finish
- 2008-11-01
- Last updated by the study team
- 2008-11-24
Who can join
Age: 21 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Males or females > 21 years old
- Scheduled to undergo bilateral LASIK
- Likely to complete all study visits and able to provide informed consent
You may not qualify if…
- Prior or current use of topical cyclosporine within the last 1 year
- Known contraindications to any study medication or ingredients
- Ocular disorders
- Active ocular diseases or uncontrolled systemic disease
- Active ocular allergies
- Complications at the time of surgery
Where it is running
- Ophthalmic Consultants of long Island — Rockville Centre, New York, United States
Full record on ClinicalTrials.gov
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