A Clinical Study of Systane® Lid Wipes in Brazil

Alcon

Status: Completed

Conditions: Skin Tolerance; Ocular Tolerance

Treatments: Other: Systane® Lid Wipes

Study type: Interventional

Funder types: Industry; Other

Identifiers

NCT02380261

EXR338-P001

Details and patient eligibility

About

The purpose of this study is to verify the skin and ocular tolerance of the product Systane® Lid Wipes.

Enrollment: 35 patients

Sex: All

Ages: 18 to 70 years old

Volunteers: Accepts Healthy Volunteers

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.

Trial design

35 participants in 1 patient group

Systane

Experimental group

Description:

Systane® Lid Wipes, 1 per eyelid, used once and discarded after each use, for 21 days

Treatment:

Other: Systane® Lid Wipes