MedPath

Evaluation of Satisfaction Regarding Patient's Management of Ocular Surface Diseases

Phase 4
Completed
Conditions
Eyelid Diseases
Registration Number
NCT01091311
Lead Sponsor
Laboratoires Thea
Brief Summary

Multicentric study, open label, uncontrolled phase IV in 30 patients with meibomian glands dysfunction .

Its objective is to Collect information from patients and ophthalmologists specialized in ocular surface and eyelids to anticipate how Blephasteam ® can be optimized.

This study involves 2 visits, visit of Inclusion, J0, then end of study visit, D21.

Between the two visits patients will be treated with Blephasteam ® for 21 days (up to two uses per day) and complete a questionnaire every two days during the first week and then once a week the next two weeks.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (3)

C.H.N.O des XV-XX

🇫🇷

Paris, France

Hôpital Bichat - Claude Bernard

🇫🇷

Paris, France

Hôpital Gabriel Montpied

🇫🇷

Clermont-Ferrand, France

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