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Withdrawn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

• 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

Study Timeline

• Study First Submitted: 2012-03-02
• Study First Submitted QC: 2012-03-02
• Study First Posted: 2012-03-07
• Status Verified: 2015-08
• Last Update Submitted: 2015-08-31
• Last Update Posted: 2015-09-02

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• Status: WITHDRAWN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

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.

Trial Locations

Locations (1)

Augenklinik; 🇩🇪 Berlin, Germany