Retina Associates of Cleveland, Inc. : Research/Clinical Trials

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Clinical Trials and Research
We feel strongly about participation in clinical research and are dedicated to exploring newer and better treatment options for our patients. Our physicians and nurses are available to discuss participation in clinical trials and whether it is right for you.
Diane W., RN, BSN
Diane graduated from BGSU, working 7 yrs in Med/Surg and Home Care, then 15 yrs at Mt. Sinai as a Clinical Specialist/Practice Manager of the Eye Clinic and coordinator for the Ophthalmology Residency program. Diane joined RACI in 1999 and serves as the Sr. Clinical Nurse and Study Coordinator.
Kimberly D., LPN, CCRP
Kimberly has worked in ophthalmology since 1984, and started at Retina Associates of Cleveland in 1994. While at Retina Associates she has worked as a Technician assisting the physicians, coordinated multiple clinical trials and manages the Low Vision Resource Center, located in the Beachwood office.
Dianne H., RN, BSN, CCRC
Dianne has been an RN since 1984. She started clinical research with the Cleveland Clinic in 1997, and in 1991 received her certification as a Clinical Research Nurse. Dianne joined Retina Associates of Cleveland in 2006. She has personally coordinated over 50 clinical trials.
Lori R., COA
Lori is a Certified Ophthalmic Assistant and has worked for RACI since 1990. She is a Photographer/Technician who has worked with several clinical trials over the years as both a Clinic Coordinator and Study Photographer.
Larraine (Rae) S., RN, BA, CCRC
Larraine (Rae) S., RN, BA, CCRC has been an RN since 1984 and a Clinical Research Nurse since 1988. Rae also holds a BBA from Baldwin Wallace. She was employed by UH for 17 years with experience in multiple disciplines and the Cleveland Clinic for 5 years. Rae joined RACI in 2007 and is certified as a Clinical Research Coordinator.
Susan R., PA-C
Susan has been working at RACI since 1988. She has worked in the office, operating room, and in clinical research, and for the last 10 years has had a main focus in Clinical Drug Research. Susan said that the most gratifying aspect of clinical drug research is participating in a study in which the drug proves to be beneficial for patients and obtains FDA approval.
Tammy B., MA/COA
Tammy has been with Retina Associates of Cleveland since 2001 as clinical technician/study refractor/study coordinator. She worked in general ophthalmology for 10 years prior to joining RACI.
Trina N., COT
Trina has been working in Ophthalmology since 1991. She has been employed with Retina Associates of Cleveland since 2003. Her background in Ophthalmology includes working as a Technician, a Clinical Research Coordinator and as a Study Photographer. Trina likes to be active in local and national ophthalmology organizations.
Vivian T., CCRP, COT
Vivian has been a Certified Clinical Research Professional since 2003. In addition, she has experience in multiple disciplines: 33 years experience as a Certified Ophthalmic Technician, 25 years experience as a Clinical Research Coordinator, 18 years experience as an Ultra-sonographer and 25 years as an Electroretinographer. Vivian has been with Retina Associates of Cleveland since 1993.

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Age-related Macular Degeneration

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Retinal Vein Occlusion

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Research & Clinical Trials

Study Detail: Lucentis and Psychological morbidity in Retinal Vein Occlusion

Trial Description Summary : To study the psychological impact of vein occlusions. There will be two groups. One group of patients, with active disease, will be treated with Lucentis for 6 months and answer questionnaires. The second group, with inactive disease, will just complete questionniares.

Basic Trial Information
Phase: III
Disease:Vein Occlusion (either central retinal or branch)
Sponsor: Genentech
Protocol Number: FVF4638s
Status: Enrolling

Study Duration: 6 months

Eligibility Criteria:
Inclusion Criteria
        CRVO in all 4 quadrants with dilated veins OR BRVO on clinical exam
        BCVA 20/40-20/8,000 inclusive
        OCT greater than, or equal to, 250 microns
         No previous treatment that might compromise or confound assessment of the study outcomes

   Exclusion Criteria
         History of any laser in study eye
          History of vitreal surgery
          Previous treatment (either eye) with
                           triamcinolone
                          bevacizumab
                           pegaptabnib
                           ranibizumab
         CVA less that 1 year before study enrollment

The above inclusion/exclusion criteria is not complete and the study coordinator will do a complete screening.

Study Title : Impact of Lucentis on psychological morbidity in patients with macular edema and neovascularization secondary to retinal vein occlusion

Trial Contact Information
Site: Beachwood
Study Coordinator: Dianne H 216/831-5704 extension 253

Clinical Trials and Research

Diane W., RN, BSN

Kimberly D., LPN, CCRP

Dianne H., RN, BSN, CCRC

Lori R., COA

Larraine (Rae) S., RN, BA, CCRC

Susan R., PA-C

Tammy B., MA/COA

Trina N., COT

Vivian T., CCRP, COT