Expired Study
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Fort Worth, Texas 76134


Purpose:

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.


Study summary:

Required follow-up for this study is 3 months post treatment.


Criteria:

Inclusion Criteria: - 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. Exclusion Criteria: - 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.


NCT ID:

NCT02477605


Primary Contact:

Study Director
Clinical Manager, Surgical, GCRA
Alcon, A Novartis Division


Backup Contact:

N/A


Location Contact:

Fort Worth, Texas 76134
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 21, 2020

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