Assessment of Patient's Satisfaction Regarding the Handiness of Two Hyaluronic Acid Eye Drops Vials
Not Applicable
Withdrawn
- Conditions
- Assess the Patient Feeling About the Handiness of Two Different Vials Used to Deliver Both, Unpreserved Hyaluronic Eye Drops
- Interventions
- Device: HYABAK®Device: HYLO-COMOD®
- Registration Number
- NCT01546012
- Lead Sponsor
- Laboratoires Thea
- Brief Summary
Assess the patient feeling about the handiness of two different vials used to deliver both, unpreserved hyaluronic eye drops.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- WITHDRAWN
- Sex
- All
- Target Recruitment
- Not specified
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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description HYABAK® HYABAK® Hyaluronic Acid eye drops CE marked, packaged in multidose ABAK® container (preservative free) HYLO-COMOD®: HYLO-COMOD® Hyaluronic Acid eye drops CE marked, packaged in multidose COMOD® container (preservative free)
- Primary Outcome Measures
Name Time Method 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.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Augenklinik
🇩🇪Berlin, Germany