Assessment of Patient's Satisfaction Regarding the Handiness of Two Hyaluronic Acid Eye Drops Vials

Thea Pharma

Status: Withdrawn

Conditions: Assess the Patient Feeling About the Handiness of Two Different Vials Used to Deliver Both, Unpreserved Hyaluronic Eye Drops

Treatments: Device: HYABAK®; Device: HYLO-COMOD®

Study type: Interventional

Funder types: Industry

Identifiers

NCT01546012

2012-001233-14 (EudraCT Number)

LT1550-PIV-CE-10/11

Details and patient eligibility

About

Assess the patient feeling about the handiness of two different vials used to deliver both, unpreserved hyaluronic eye drops.

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Man or woman aged 18 and older
• Patient with dry eye for at least 3 months
• Having given his written informed consent

Exclusion criteria

• Intolerance to studied products
• Patient's inability to understand the study procedures and give informed consent.
• Patient unwilling to follow the study procedures and visits defined by the protocol.
• Pregnant or lactating women.
• Patient under guardian ship

Trial design

0 participants in 2 patient groups

HYABAK®

Experimental group

Description:

Hyaluronic Acid eye drops CE marked, packaged in multidose ABAK® container (preservative free)

Treatment:

Device: HYABAK®

HYLO-COMOD®:

Active Comparator group

Description:

Hyaluronic Acid eye drops CE marked, packaged in multidose COMOD® container (preservative free)

Treatment:

Device: HYLO-COMOD®