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

Status

Withdrawn

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT01546012

Enrollment

Registered

2012-03-07

Start date

Unknown

Completion date

Unknown

Last updated

2015-09-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

Brief summary

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

Interventions

DEVICEHYABAK®

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

DEVICEHYLO-COMOD®

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

Study design

Allocation

RANDOMIZED

Intervention model

CROSSOVER

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

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

Design outcomes

Primary

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

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026