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Microperimetry and Optical Coherence Tomography (OCT) With Lucentis for Diabetic Macular Edema (DME) (MORE)

Primary Purpose

Diabetic Macular Edema

Status
Unknown status
Phase
Phase 2
Locations
Austria
Study Type
Interventional
Intervention
Ranibizumab
Sponsored by
The Ludwig Boltzmann Institute of Retinology and Biomicroscopic Laser Surgery
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Macular Edema focused on measuring Clinically Significant Diabetic Macular Edema, Focal Laser, GRID-Laser, Ranibizumab, Lucentis, Microperimetry, High-Definition OCT, Randomized, Observer-Blinded, Ineffective Treatment with Focal Laser or GRID-Laser

Eligibility Criteria

51 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Study eye with clinically significant macular edema, for which one of the following characteristics has to be present:
  • retinal thickening at or within 500µm from the center of the macula,
  • hard exudates at or within 500µm from the center of the macula associated with thickening of the adjacent retina,
  • a zone (>1-disk area) or zones of retinal thickening of which any part is within 1 disk diameter from the center of the macula.
  • Second line treatment after ineffective laser treatment
  • Men or women with diabetes mellitus
  • Only one eye per patient
  • Age > 50 years
  • HbA1c < 8%

Exclusion Criteria:

  • Study eye with concomitant retinal or choroidal disorder other than diabetic retinopathy
  • Study eye with significant central lens opacities and / or conditions that limit the view of the fundus
  • poor general condition
  • woman of childbearing potential, current pregnancy or breastfeeding
  • Patients who are unwilling to adhere to visit examination schedules
  • Evidence of macular traction or taut posterior hyloid.

Sites / Locations

  • Rudolf Foundation Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

0.5 mg Ranibizumab

1.0 mg of Ranibizumab

Arm Description

3 intravitreal injections of 0.5 mg Ranibizumab every 5 weeks

3 intravitreal injections of 1.0mg Ranibizumab every 5 weeks

Outcomes

Primary Outcome Measures

Retinal thickness

Secondary Outcome Measures

Retinal sensitivity
Distance best corrected visual acuity
Reading best corrected visual acuity
Intraocular pressure
Type of diabetic macular edema
Type of diabetes mellitus HbA1c
Blood-pressure
Age

Full Information

First Posted
April 20, 2009
Last Updated
June 23, 2011
Sponsor
The Ludwig Boltzmann Institute of Retinology and Biomicroscopic Laser Surgery
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1. Study Identification

Unique Protocol Identification Number
NCT00885794
Brief Title
Microperimetry and Optical Coherence Tomography (OCT) With Lucentis for Diabetic Macular Edema (DME)
Acronym
MORE
Official Title
Microperimetry and High-Definition-OCT in Ranibizumab Treatment for Diabetic Macular Edema (MORE-Study)
Study Type
Interventional

2. Study Status

Record Verification Date
June 2011
Overall Recruitment Status
Unknown status
Study Start Date
May 2008 (undefined)
Primary Completion Date
May 2011 (Actual)
Study Completion Date
May 2012 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
The Ludwig Boltzmann Institute of Retinology and Biomicroscopic Laser Surgery

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Diabetic maculopathy is the leading cause of visual impairment in the working-age population in developed countries. Diabetic macular edema can cause impaired visual acuity and so far is treated by laser, vitreous surgery, and intravitreal cortisone application. Still 50% of the cases do not respond to the treatment. Recently intraocular anti-VEGF-treatment with ranibizumab (Lucentis®, Novartis) in diabetic macular edema has proven efficacy to last over a period of 3 to 6 months. Still, the optimal dosage for those intravitreal injections still has to be found, because frequent injections are necessary. The measurement of visual acuity is inadequate to quantify in detail the visual impairment. Using the newest technology of a high-definition optical coherence tomography (Cirrus-OCT, Carl Zeiss Meditec Inc.) to determine the retinal thickness, and a miroperimetry (MP-1, Nidek Technologies) to determine retinal sensitivity, we hope to find the optimal dosage of intravitreal anti-VEGF treatment in diabetic macular edema. Study objective: To determine the dose response of 0.5mg and 1.0mg ranibizumab (Lucentis®, Novartis Pharma) intravitreal injection in subjects with resistant diabetic macular edema and evaluate safety and tolerability.
Detailed Description
Diabetic maculopathy due to diabetic macular edema (DME) is the leading cause of visual impairment in the working-age population in developed countries. DME is the swelling of the retina resulting from the exudation and accumulation of extracellular fluid and proteins in the macula. Structural changes in the endothelium of retinal vessels lead to a breakdown of the blood-retina barrier and increase vascular permeability, resulting in exudation. The standardized treatment of DME is a focal laser or GRID-laser treatment with or without combined triamcinolone intravitreal injections. Those laser treatments produce scars in the central retina and are not always very effective. In cases of macular traction or taut posterior hyloid vitrectomy and retinal surgery are necessary. Vascular endothelial growth factor (VEGF) has been implicated as an important factor in the occurrence of vascular permeability in DME. In patients with DME, VEGF levels are significantly elevated, compared to patients without ocular disease. Therefore, anti-VEGF treatment has been implicated as an important treatment of DME and recently intraocular anti-VEGF-treatment with ranibizumab (Lucentis®, Novartis Pharma) in diabetic macular edema has proven to be very effective. Just like in patients with age-related macular degeneration (AMD), anti-VEGF treatment was given 3 times every 4-6 weeks. The same treatment was repeated at a relapse of the disease, again 3 times every 4-6 weeks. One study group treated DME with 0.5mg ranibizumab intravitreal injections and the other compared 0.3mg to 0.5mg of ranibizumab intravitreal injections. An optimal treatment dose has not been found yet. Visual acuity assessment is currently used to determine the functional damage caused by edema, although it may not completely describe the functional condition of the patient. Furthermore, visual acuity alone does not seem to be the best parameter to define the effect and continuation of treatment. Retinal thickness, as measured by the noninvasive optical coherence tomography (OCT) can deliver detailed information about the retinal situation during and after treatment. Also a fundus related perimetry, known as microperimetry (MP), is a useful noninvasive examination method in determining the site of relative and absolute scotomas and also fixation characteristics. With MP the macular sensitivity can be measured to further assess the macular condition. Using the newest technology of a high-definition OCT (Cirrus-OCT, Carl Zeiss Meditec Inc.) to determine the retinal thickness, and a MP with automated correction for eye movements (MP-1, Nidek Technologies) to determine retinal sensitivity, we intend to analyze this new treatment option for DME, and find the optimized dose for intravitreal injection of ranibizumab in cases of ineffective laser treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Macular Edema
Keywords
Clinically Significant Diabetic Macular Edema, Focal Laser, GRID-Laser, Ranibizumab, Lucentis, Microperimetry, High-Definition OCT, Randomized, Observer-Blinded, Ineffective Treatment with Focal Laser or GRID-Laser

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Single Group Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
0.5 mg Ranibizumab
Arm Type
Experimental
Arm Description
3 intravitreal injections of 0.5 mg Ranibizumab every 5 weeks
Arm Title
1.0 mg of Ranibizumab
Arm Type
Experimental
Arm Description
3 intravitreal injections of 1.0mg Ranibizumab every 5 weeks
Intervention Type
Drug
Intervention Name(s)
Ranibizumab
Other Intervention Name(s)
Lucentis
Intervention Description
3 intravitreal injection every 5 weeks
Primary Outcome Measure Information:
Title
Retinal thickness
Time Frame
at 3 months
Secondary Outcome Measure Information:
Title
Retinal sensitivity
Time Frame
3, 6, and 9 months
Title
Distance best corrected visual acuity
Time Frame
3, 6, and 9 months
Title
Reading best corrected visual acuity
Time Frame
3, 6, and 9 months
Title
Intraocular pressure
Time Frame
3, 6, and 9 months
Title
Type of diabetic macular edema
Time Frame
3, 6, and 9 months
Title
Type of diabetes mellitus HbA1c
Time Frame
3, 6, and 9 months
Title
Blood-pressure
Time Frame
3, 6, and 9 months
Title
Age
Time Frame
3, 6, and 9 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
51 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Study eye with clinically significant macular edema, for which one of the following characteristics has to be present: retinal thickening at or within 500µm from the center of the macula, hard exudates at or within 500µm from the center of the macula associated with thickening of the adjacent retina, a zone (>1-disk area) or zones of retinal thickening of which any part is within 1 disk diameter from the center of the macula. Second line treatment after ineffective laser treatment Men or women with diabetes mellitus Only one eye per patient Age > 50 years HbA1c < 8% Exclusion Criteria: Study eye with concomitant retinal or choroidal disorder other than diabetic retinopathy Study eye with significant central lens opacities and / or conditions that limit the view of the fundus poor general condition woman of childbearing potential, current pregnancy or breastfeeding Patients who are unwilling to adhere to visit examination schedules Evidence of macular traction or taut posterior hyloid.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ulrike Stolba, MD
Organizational Affiliation
Department of Ophthalmology, Ludwig Boltzmann Institute for Retinology and Biomicroscopic Lasersurgery, Rudolf Foundation Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rudolf Foundation Clinic
City
Vienna
ZIP/Postal Code
1030
Country
Austria

12. IPD Sharing Statement

Learn more about this trial

Microperimetry and Optical Coherence Tomography (OCT) With Lucentis for Diabetic Macular Edema (DME)

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