Trials / Terminated
TerminatedNCT02511379
Clinical Evaluation of Systane® Balance in Dry Eye Subjects
Clinical Evaluation of Systane® Balance on Corneal Staining in Indian Subjects With Dry Eye
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 14 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the efficacy and safety of Systane® Balance following 90 days of QID (4 times/day) dosing among Indian subjects with dry eye.
Detailed description
This study was conducted in India.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Propylene Glycol 0.6% eye drops |
Timeline
- Start date
- 2015-11-26
- Primary completion
- 2016-06-20
- Completion
- 2016-06-20
- First posted
- 2015-07-30
- Last updated
- 2018-10-31
- Results posted
- 2018-09-05
Source: ClinicalTrials.gov record NCT02511379. Inclusion in this directory is not an endorsement.