Tear Dynamics After Restasis Treatment in Dry Eye Patients
Completed
Conditions studied: Dry Eye
In brief
Observe the changes of tear volume in dry eye patients after Restasis treatment of 3 months and during 6-month follow-up after discontinuation of study treatment.
Key facts
- Study ID
- NCT00706940
- Run by
- University of Miami
- People needed
- 60
- Starts
- 2011-08-01
- Expected to finish
- 2016-12-31
- Last updated by the study team
- 2017-04-25
Who can join
Age: 18 and older, up to 90. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- The participant will be eligible for entry in the study if s/he:
- Is at least 18 years old and has full legal capacity to volunteer;
- Has read and signed the IRB Informed Consent Document;
- Is willing and able to follow participant instructions;
- Has clear corneas;
- Has 20/100 uncorrected visual acuity or better;
- Has dry eye according to the study definition of DES (study subjects);
- Has not use Restasis within 3 months.
You may not qualify if…
- The subjects will ineligible for entry into the study if s/he:
- Has any systemic disease affecting ocular health except for Sjögren's syndrome;
- Is using any systemic or topical medications that will affect ocular health except for artificial tears;
- Has an active ocular disease other than DES, or Sjögren's syndrome
- Has any clinically significant lid or conjunctival abnormalities, neovascularization, corneal scars or corneal opacities;
- Has limbal or bulbar injection or corneal staining that was clinically significant, which are not due to DES;
- Has worn rigid gas permeable lenses within 1 year and during the study;
- Has had surgery or an eye injury within 6 months;
- Was a soft contact lens wearer within 2 weeks and during the study.
Where it is running
- Bascom Palmer Eye Institute — Miami, Florida, United States
Full record on ClinicalTrials.gov
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