Clinical Evaluation of Systane® Balance in Dry Eye Subjects
- Conditions
- Health Condition 1: null- Dry Eye
- Registration Number
- CTRI/2015/10/006320
- Lead Sponsor
- Alcon laboratories India pvt Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Other (Terminated)
- Sex
- Not specified
- Target Recruitment
- 14
1. Sign Informed Consent and willing and able to attend all study visits
2. Dry eye in both eyes diagnosed by an ophthalmologist
3. Other protocol-specified inclusion criteria may apply
1. Women of childbearing potential who are pregnant or breast feeding.
2. Any medical condition (systemic or
ophthalmic) that may preclude the safe
administration of test article or safe participation in the study
3. Ocular surgery or ocular trauma requiring medical or pharmacological treatment
within 1 year of Screening
4. Use of topical ocular prescription or non-prescription medications, RESTASIS or topical ocular steroids within 14 days of screening
5. Use of any artificial tears/gels/lubricants/rewetting drops within 4 hours of screening
6. Contact lens wear within 1 week of Screening and/or unwillingness to discontinue contact lens wear for the duration of the study
7. Other protocol-specified exclusion criteria may apply
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method