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Clinical Trials/NCT01546012
NCT01546012
Withdrawn
Not Applicable

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

Laboratoires Thea1 site in 1 countryMarch 7, 2012
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ConditionsAssess the Patient Feeling About the Handiness of Two Different Vials Used to Deliver Both, Unpreserved Hyaluronic Eye Drops

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Assess the Patient Feeling About the Handiness of Two Different Vials Used to Deliver Both, Unpreserved Hyaluronic Eye Drops
Sponsor
Laboratoires Thea
Locations
1
Primary Endpoint
Overall preference of the patient
Status
Withdrawn
Last Updated
10 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

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

Registry
clinicaltrials.gov
Start Date
March 7, 2012
End Date
TBD
Last Updated
10 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

Overall preference of the patient

Time Frame: 6 weeks

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

Study Sites (1)

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