Tear Film Thickness Clinical Trial
NCT number | NCT00469521 |
Other study ID # | 5304 |
Secondary ID | |
Status | Completed |
Phase | Phase 4 |
First received | May 2, 2007 |
Last updated | September 5, 2007 |
Verified date | September 2007 |
Source | Innovative Medical |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States:Institution Review Board |
Study type | Interventional |
To determine baseline tear thickness and improvement immediately post installation of two artificial tear solutions:(9582X) and Allergan Refresh Tears.
Status | Completed |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: 1. Normal, healthy volunteers 18 years or older 2. Males or females 3. Any race or ethnic background Exclusion Criteria: 1. Corneal refractive surgery within 6 months of this study. 2. Contact lens use on day of examination. 3. Corneal ectasia |
Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label
Country | Name | City | State |
---|---|---|---|
United States | Magill Research Center Institute MUSC | Charleston | South Carolina |
Lead Sponsor | Collaborator |
---|---|
Innovative Medical |
United States,
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT02713399 -
High-resolution Imaging of Tear Film Thickness in Contact Lenses Wearers With Optical Coherence Tomography (OCT). A Pilot Study
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