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

NCT01189474 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 104

Last updated 2012-10-03

No results posted yet for this study

Summary

Multicentric study, open label, uncontrolled phase IV in 140 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.

Conditions

  • Eyelid Diseases

Interventions

DEVICE

Blephasteam

Eye lid warming goggles

Sponsors & Collaborators

  • Laboratoires Thea

    lead INDUSTRY

Principal Investigators

  • Jean Paul ADENIS, Professor · Hopital Dupuytren Limoges

  • Isabelle BADELLON, Doctor · Fondation Rothschild Paris

  • Vincent BORDERIE, Professor · CHNO des quinze-vingts

  • Tristan BOURCIER, Professor · CHU de Strasbourg

  • Jean Louis BOURGES, Doctor · Hotel Dieu Paris

  • Dominique BREMOND GIGNAC, Professor · Centre Hospitalier Universitaire, Amiens

  • Carole BURILLON, Professor · Hopital Edouard Heriot Lyon

  • Philippe CAZEMIND, Doctor · Clinique du cours Dillion

  • Hervé CHENAL, Doctor

  • Joseph COLIN, Professor · University Hospital, Bordeaux

  • Catherine CREUZOT GARCHER, Professor · Centre Hospitalier Universitaire Dijon

  • Stephan FAUQUIER, Doctor

  • Denis FLORES, Doctor

  • Philippe GAIN, Professor · CHU de Saint Etienne

  • Olivier Galatoire, Doctor · Fondation Rothschild Paris

  • Damien GATINEL, Doctor · Fondation Rothschild Paris

  • Jean Luc GEORGES, Professor · Central Hospital, Nancy, France

  • Thanh HOANG XUAN, Professor

  • Philippe IMBERT, Doctor · Polyclinique du Parc

  • Marc LABETOULLE, Professor · CH de Bicetre

  • Karim LAOUAR, Doctor · Centre Hospitalier de Nimes

  • Sylvie MAES CASTELLARIN, Doctor · Hopital de Tarbes

  • Sylvie MAINGUY, Doctor

  • Claire MEURIOT TUIL, Doctor

  • Solange MILAZZO, Professor · Centre Hospitalier Universitaire, Amiens

  • Bruno MORTEMOUSQUE, Doctor · University Hospital, Bordeaux

  • Pierre Jean PISELLA, Professor · CHU de Tours

  • Pierre Yves ROBERT, Professor · University Hospital, Limoges

  • Stephane RONCIN, Doctor · Polyclinique Saint Laurent

  • Jean François ROULAND, Professor · CHU de Lille

  • Pierre LABALETTE, Professor · CHU de Lille

  • Frank ROUX, Doctor · HIA Laveran

  • Claude SPEEG, ¨Professor · CHU de Strasbourg

  • Michel TAZARTES, Doctor

  • Yves UTEZA, Doctor

  • Hatem ZEGHIDI, Doctor

  • Benoit BRIAT, Doctor

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
4 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-06-30
Primary Completion
2011-12-31
Completion
2011-12-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01189474 on ClinicalTrials.gov