Home
Search
Study Topics
Glossary
|
|
|
|
|
Sponsored by: |
Alcon Research |
---|---|
Information provided by: | Alcon Research |
ClinicalTrials.gov Identifier: | NCT00809198 |
The effect of Kynex versus Refresh Plus in subjects with mild to moderate dry eye.
Condition | Intervention | Phase |
---|---|---|
Dry Eye |
Drug: Kynex Drug: Refresh Plus |
Phase IV |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Single Blind (Investigator), Parallel Assignment |
Official Title: | The Effect of Kynex Versus Refresh Plus in Subjects With Mild to Moderate Dry Eye - A Parallel Group, Randomized, Masked Study |
Estimated Enrollment: | 78 |
Study Start Date: | December 2008 |
Estimated Primary Completion Date: | October 2009 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
---|---|
1: Experimental
Sodium Hyaluronate (Kynex)
|
Drug: Kynex |
2: Active Comparator
Carboxymethylcellulose sodium (Refresh Plus)
|
Drug: Refresh Plus |
Ages Eligible for Study: | 20 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Alcon Call Center | 1-888-451-3937 | medical.information@alconlabs.com |
United States, Texas | |
Alcon Call Center for Trial Locations | Recruiting |
Fort Worth, Texas, United States, 76134 | |
Contact: Hyesung Shin +82 2 2007 5000 Hyesung.shin@alconlabs.com |
Responsible Party: | Alcon Korea Ltd. ( Hyesung Shin\Clinical Research Associate ) |
Study ID Numbers: | RM-08-06 |
Study First Received: | December 16, 2008 |
Last Updated: | December 16, 2008 |
ClinicalTrials.gov Identifier: | NCT00809198 History of Changes |
Health Authority: | Korea: IRB |
Sodium Hyaluronate, Kynex, Carboxymethylcellulose sodium Refresh Plus Dry Eye Cornea Staining TBUT |
Corneal Diseases Hyaluronic Acid |