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

Completed

Conditions studied: Vitrectomy

In brief

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

Key facts

Study ID

NCT01319318

Run by

Allergan

People needed

25

Starts

2011-03-01

Expected to finish

2012-06-01

Last updated by the study team

2013-07-02

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Require pars plana vitrectomy in at least 1 eye
• Best corrected visual acuity in the study eye between 20/400 and 20/40

You may not qualify if…

• Use of any NSAIDs (topical or systemic) within 14 days
• Use of topical or systemic steroids within 30 days
• Active eye infection in either eye
• Any eye surgery within 6 months
• Prior pars plana vitrectomy, YAG capsulotomy or uveitis

Where it is running

• Study site — San Antonio, Texas, United States

Full record on ClinicalTrials.gov

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