Safety and Efficacy of Intravitreal Fluocinolone Acetonide Implants in Patients With Diabetic Macular Edema

NCT ID: NCT00576459

Last Updated: 2011-12-08

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2003-03-31
• Study Completion Date: 2006-07-31

Brief Summary

This is a 3-year randomized, dose masked, three-arm controlled, pilot study to evaluate the safety and efficacy of the intravitreal FA implants (0.59mg and 2.1mg), when compared to laser photocoagulation in the treatment of patients with diabetic macular edema.

Conditions

Diabetic Macular Edema

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Fluocinolone acetonide 0.59 mg

0.59 mg fluocinolone acetonide intravitreal implant

Group Type: EXPERIMENTAL

0.59 mg fluocinolone acetonide intravitreal implant

Intervention Type: DRUG

0.59 mg

Fluocinolone acetonide 2.1 mg

2.1 mg fluocinolone acetonide intravitreal implant

Group Type: EXPERIMENTAL

2.1 mg fluocinolone acetonide intravitreal implant

Intervention Type: DRUG

2.1 mg

Laser photocoagulation

standard of care laser photocoagulation

Group Type: ACTIVE_COMPARATOR

standard of care laser photocoagulation

Intervention Type: PROCEDURE

standard of care laser photocoagulation

Interventions

0.59 mg fluocinolone acetonide intravitreal implant

0.59 mg

Intervention Type: DRUG

2.1 mg fluocinolone acetonide intravitreal implant

2.1 mg

Intervention Type: DRUG

standard of care laser photocoagulation

standard of care laser photocoagulation

Intervention Type: PROCEDURE

Other Intervention Names

Retisert

Eligibility Criteria

Inclusion Criteria

• Subjects with type 1 or 2 diabetes.
• Subjects with clinically significant macular edema as defined by the ETDRS.
• A best corrected visual acuity between +0.30 and +1.00 logMAR (70 and 35 letters or approximately 20/40 to 20/200) as measured on an ETDRS chart.
• Subjects with laser treatment status/history as follows: [1] Naïve to laser photocoagulation or Focal laser photocoagulation more than 16 weeks prior to screening or PRP more than 24 weeks prior to screening, [2] No laser scars within 500µm (4x the width of a retinal vein at the disc margin) of the central macula.
• The subject's ocular media had to be sufficiently clear to allow for quality fundus photography.
• If aphakic or pseudophakic, lens removal had to have occurred at least 40 weeks prior to screening.
• Subjects had to be males or non-pregnant females of at least 18 years.
• Subjects had to display the ability and willingness to comply with treatment, follow up process, and sign an Informed Consent Form.

Exclusion Criteria

• Subjects who have had previous grid macular photocoagulation for diffuse macular edema.
• Presence of posterior hyaloid membrane, epiretinal membranes, fibrovascular proliferation, and vitreopapillary traction, which causes tractional distortion on the macula as demonstrated by OCT or funduscopy.
• History of or current retinal detachment requiring surgical treatment or a scleral buckle.
• Diabetic Retinopathy that required immediate PRP.
• Ocular disease other than diabetic retinopathy that could confound the outcome of the study (e.g., age-related macular degeneration, drug toxicity, uveitis, hypertensive retinopathy, ischemic maculopathy, etc.).
• Glaucoma, or history of glaucoma in either the study eye or the fellow eye.
• Ocular hypertension, or history of ocular hypertension requiring IOP lowering treatment.
• A media opacity that precludes visualization and/or diagnosis of the status of the eye.
• Concurrent coumadin therapy or known bleeding diathesis.
• Subjects requiring chronic systemic corticosteroid therapy or systemic immunosuppressive therapy to manage non-ocular disease.
• Concurrent treatment with a new investigational drug.
• Subjects with a best-corrected visual acuity worse than +1.0 logMAR (20/200 or 35 ETDRS letters) in the fellow eye.
• Pregnant or lactating females.
• Females of childbearing potential considering becoming pregnant during the course of the study and those not taking effective contraception/precautions to avoid pregnancy.
• History of hypersensitivity to fluorescein, known allergies to steroids or any component of the intraocular device.
• Subjects with photophobia that will preclude the ability to do fundus evaluations.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Bausch & Lomb Incorporated

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Taraprasad Das, MD

Role: PRINCIPAL_INVESTIGATOR

LV Prasad Eye Institute

Dennis Lam Shun-Chiu, MD

Role: PRINCIPAL_INVESTIGATOR

Chinese University of Hong Kong

Locations

The Chinese University of Hong Kong

Hong Kong, , China

LV Prasad Eye Institute

Banjara Hills, Hyderabad, India

Countries

China; India

Other Identifiers

420-003

Identifier Type: -

Identifier Source: org_study_id