Trials / Completed
CompletedNCT00883649
Efficacy and Safety Study of Nutritional Supplements for Treatments of Dry Eye
A Randomized, Parallel-Group, Placebo-Control, Double-Blind Trial Comparing the Efficacy and Safety of Nutritional Supplementation Containing Omega 3 Fatty Acids and Gamma Linoleic Acid, for Treatment of Keratoconjunctivitis Sicca in Post-Menopausal Females
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 62 (actual)
- Sponsor
- Virginia Eye Consultants · Academic / Other
- Sex
- Female
- Age
- 40 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine the effectiveness of a nutritional supplement in post-menopausal women age 40 or older with moderate to severe dry eyes. This study is being conducted to determine if signs and symptoms of dry eye will improve with the use of this nutritional supplement.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Hydroeye | 2 Capsules BID |
| OTHER | Inactive Capsule | 2 Capsules BID |
Timeline
- Start date
- 2008-09-01
- Primary completion
- 2011-12-01
- First posted
- 2009-04-20
- Last updated
- 2012-02-20
Locations
2 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00883649. Inclusion in this directory is not an endorsement.