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Dosage Study for Vigamox Eye Drops Prior to Intravitreal Injections

Information source: Illinois Retina Associates
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Intravitreal Injection Patients

Intervention: Vigamox (Drug)

Phase: Phase 4

Status: Not yet recruiting

Sponsored by: Illinois Retina Associates

Official(s) and/or principal investigator(s):
Kourous A Rezaei, MD, Principal Investigator, Affiliation: Illinois Retina Associates SC

Overall contact:
Kourous A Rezaei, MD, Phone: 708-596-8710, Email: karezaei@yahoo.com


Antibiotic eye drops are being used before and after intravitreal injections. Currently there is no study indicating the benefit of there usage or their dosage. In this study we compare the efficacy of Vigamox eye drops (antibiotic)starting 3 days prior to the injection versus 1 day prior to intravitreal injection.

Clinical Details

Official title: To Compare the Efficacy of Topical Vigamox Eye Drops at Tid 3 Days Prior to Intravitreal Injection Versus Tid 1 Day Prior to Intravitreal Injection

Study design: Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Primary outcome: Timed study


Minimum age: 21 Years. Maximum age: N/A. Gender(s): Both.


Inclusion Criteria:

- Patient who need intravitreal injections patients who are willing to participate in

the study Exclusion Criteria:

- Patients who are allergic to Vigamox or who have taken any eye drops within the past

3 weeks

Locations and Contacts

Kourous A Rezaei, MD, Phone: 708-596-8710, Email: karezaei@yahoo.com

Illinois Retina Associates, Harvey, Illinois 60426, United States; Not yet recruiting
David J Baczewski, Phone: 708-915-6808, Email: davidb@illinoisretina.com
Kourous A Rezaei, MD, Principal Investigator
Additional Information

Starting date: July 2008
Last updated: June 3, 2008

Page last updated: August 23, 2015

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