Observational Study to Assess the Effect of Iluvien® in DME Patients Insufficiently Responsive to Available Therapies

NCT02080091 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 25

Last updated 2015-08-26

Study results available
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Summary

This observational study aims to assess the safety and effect of Iluvien® in DME patients considered insufficiently responsive to available therapies in a real life setting in Germany.

Conditions

  • Diabetic Macular Edema (DME)

Sponsors & Collaborators

  • Alimera Sciences

    lead INDUSTRY

Principal Investigators

  • Professor Helmut Hoeh, MD · Dietrich-Bonhoeffer-Klinikum

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-12-31
Primary Completion
2015-03-31
Completion
2015-04-30

Countries

  • Germany

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 NCT02080091 on ClinicalTrials.gov