N/A
N=35
A Clinical Study of Systane® Lid Wipes in Brazil
Ocular Tolerance · Skin Tolerance
Bottom Line
View on ClinicalTrials.gov: NCT02380261 ↗Enrolled (actual)
35
Serious AEs
0.0%
Results posted
Nov 2016
Primary outcome: Primary: Number of Participants With a Contact-dermatitis Adverse Reaction — 0 participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Systane® Lid Wipes (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Alcon Research
- Primary completion
- Oct 2015
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants With a Contact-dermatitis Adverse Reaction |
— | — |
| PRIMARY Number of Participants With Ocular Clinical Signs and Discomfort Sensations |
— | — |
Summary
The purpose of this study is to verify the skin and ocular tolerance of the product Systane® Lid Wipes.
Eligibility Criteria
Inclusion Criteria
- Must sign informed consent.
- Agree to adhere to the procedures and requirements of the study.
- Wears makeup daily.
- Other protocol-specified inclusion criteria may apply.
Exclusion Criteria
- Pregnant or breastfeeding.
- Ocular conditions as specified in protocol.
- Medical conditions as specified in protocol.
- Skin conditions as specified in protocol.
- Other protocol-specified exclusion criteria may apply.
Data sourced from ClinicalTrials.gov (NCT02380261). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.