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

Laboratoires Thea

Overview

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

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Masking

NONE

Conditions

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

Interventions

HYABAK®DEVICE

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

HYLO-COMOD®DEVICE

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

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

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

Locations (1)

Augenklinik

Berlin, Germany

Outcomes

Primary Outcomes

Overall preference of the patient

At Visit2: Week 6 +/- 1week: End of Study Visit. "Overall preference of the patient": number of answers Hyabak, Hylo-comod.

Time frame: 6 weeks

Data from ClinicalTrials.gov

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