MedTrace Logo

Efficacy and Safety of T2762 and Vismed® in Dry Eye Syndrome

NCT02023268 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 105

Last updated 2017-08-24

Study results available
· View outcomes & findings →

Summary

Comparison of the efficacy and safety of T2762 and Vismed® in the treatment of moderate to severe Dry Eye Syndrome

Conditions

  • Dry Eye Syndrome

Interventions

DEVICE

T2762

1 drop in each eye 3 to 6 times daily during 84 days

DEVICE

Vismed®

1 drop in each eye 3 to 6 times daily during 84 days

Sponsors & Collaborators

  • Laboratoires Thea

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-12-31
Primary Completion
2014-12-31
Completion
2015-02-28

Countries

  • France

Study Locations

More Related Trials

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 NCT02023268 on ClinicalTrials.gov