Observational Study of Ocular Inflammation in Patients Undergoing a Pars Plana Vitrectomy

NCT01319318 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 25

Last updated 2013-07-02

Study results available
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Summary

This study will evaluate the degree of post-operative ocular inflammation in patients who are undergoing a pars plana vitrectomy.

Conditions

  • Vitrectomy

Interventions

PROCEDURE

Pars Plana Vitrectomy

Pars plana vitrectomy performed in study eye on Day 0.

Sponsors & Collaborators

  • Allergan

    lead INDUSTRY

Principal Investigators

  • Medical Director · Allergan

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-03-31
Primary Completion
2012-06-30
Completion
2012-06-30

Countries

  • United States

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 NCT01319318 on ClinicalTrials.gov