Clinical Comparison of 27+® and 23-gauge ULTRAVIT® 7500 Cpm Vitrectomy Outcomes

Completed · Not applicable

Conditions studied: Vitreoretinal Disease

In brief

The purpose of this study is to compare the treatment day change between immediate postoperative and immediate preoperative intraocular pressure (IOP) between 27-gauge and 23-gauge vitrectomy instruments.

Key facts

Study ID

NCT02477605

Run by

Alcon Research

People needed

137

Starts

2015-07-16

Expected to finish

2016-08-31

Last updated by the study team

2018-07-02

Who can join

Age: 22 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Willing and able to provide informed consent and attend all required study visits;
• Requires vitrectomy in at least one eye;
• Other protocol-defined inclusion criteria may apply.

You may not qualify if…

• Previous vitrectomy or glaucoma surgery;
• Planned treatment requires scleral buckling, combined procedures (eg, cataract surgery), silicone oil, and expansive gas other than sterile air;
• Treated with topical IOP lowering medication(s) at any time from baseline assessment to time of surgery;
• Pregnant or planning to become pregnant during the course of the trial;
• Other protocol-defined exclusion criteria may apply.

Where it is running

• Contact Alcon Call Center for Trial Locations — Fort Worth, Texas, United States

Full record on ClinicalTrials.gov

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