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Evaluation of the Effects of Selective Photocoagulation for the Treatment of Diabetic Macular Edema (SRT)

Primary Purpose

Diabetic Macular Edema

Status
Completed
Phase
Phase 2
Locations
Israel
Study Type
Interventional
Intervention
Nd: YLF laser treatment
Sponsored by
Lumenis Be Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Macular Edema focused on measuring DME, Laser, Selective laser therapy, photocoagulation

Eligibility Criteria

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

Inclusion Criteria:

  1. Best corrected ETDRS visual acuity letter score >=24 (app. 20/320 or better)
  2. Definite retinal thickness due to diabetic macular edema by on clinical exam at or within 500 to 3000 microns of the macular center (radius) for which the investigator believes laser photocoagulation is not indicated
  3. A thickness equal or less than 315 microns in the central subfield (confirmed by SD-OCT).
  4. A thickness of >2 SD of norm in one or more inner or outer subfields on SD-OCT.
  5. Maximal focal/grid laser not yet applied (within areas of thickening between 500 and 3000 microns from center of macula, not all microaneurysms treated with direct laser and not all other areas of thickening treated with grid laser). Maximal or complete laser treatment is defined as direct treatment to all microaneurysms within areas of edema and grid treatment to all other areas of macular edema.
  6. No panretinal scatter photocoagulation (PRP) within prior 4 months.
  7. No recent medical treatment for DME (e.g., intravitreal/peribulbar steroids within past 4 months or intravitreal anti-VEGF injection within past 2 months).
  8. No major ocular surgery (including cataract extraction, any other intraocular surgery, scleral buckle, glaucoma filter, cornea transplant, etc.) within prior 6 months.
  9. No Nd:YAG laser capsulotomy within prior 2 months.
  10. Macular edema is not considered to be due to a cause other than diabetic macular edema

    o An eye should not be considered eligible (1) if the macular edema is considered to be related to cataract extraction or (2) clinical exam and/or SD-OCT suggests that vitreoretinal interface disease (eg. vitreoretinal traction or epiretinal membrane) is the primary cause of the macular edema.

  11. Media clarity, pupillary dilation, and patient cooperation sufficient for adequate fundus photos.
  12. No ocular condition (other than diabetes) that, in the opinion of the investigator, might affect macular edema or alter visual acuity during the first 12 months of the study (e.g., vein occlusion, uveitis or other ocular inflammatory disease, neovascular glaucoma, Irvine-Gass Syndrome).

    • Glaucoma per se is not an exclusion

Exclusion Criteria:

  1. History of renal failure requiring dialysis or renal transplant
  2. Condition that in the opinion of the investigator would preclude participation in the study (e.g., unstable medical status including blood pressure and glycemic control)
  3. Patients in poor glycemic control who recently (>3 months) initiated intensive insulin treatment (a pump or multiple daily injections) or plan to do so in the next 3 months should not be enrolled.
  4. A patient with only one functioning eye (i.e., letter score 0 in contra-lateral eye)

Sites / Locations

  • Tel Aviv Sourasky Medical Center
  • Sheba Medical Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Laser therapy

Arm Description

Outcomes

Primary Outcome Measures

progression of macular edema
Proportion progressing to center involved macular edema by month 12 as confirmed on SD-OCT

Secondary Outcome Measures

Full Information

First Posted
May 15, 2011
Last Updated
September 6, 2016
Sponsor
Lumenis Be Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT01355692
Brief Title
Evaluation of the Effects of Selective Photocoagulation for the Treatment of Diabetic Macular Edema
Acronym
SRT
Official Title
Phase III Multi Center Study Study of the Effects of Selective Retinal Photocoagulation for the Treatment of Diabetic Macular Edema
Study Type
Interventional

2. Study Status

Record Verification Date
September 2016
Overall Recruitment Status
Completed
Study Start Date
December 2009 (undefined)
Primary Completion Date
June 2015 (Actual)
Study Completion Date
July 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Lumenis Be Ltd.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The population of people suffering from diabetes is rapidly increasing, from an estimated 110 million in 1994 to 221 million in 2010. Diabetic macular edema is the most common reason for reduction in visual acuity in diabetic patients. The standard care for diabetic macular edema is focal and /or grid retinal photocoagulation. During photocoagulation, small laser burns are applied to the retina, the sensory tissue that lines the back of the eye. Studies have shown that photocoagulation of clinically significant diabetic macular edema substantially reduces the risk of visual loss, increase the chance of visual improvement and decrease the frequency of persistent macular edema. However, it remains unknown whether the destruction of sensory layer of the retina during photocoagulation that may cause visual field defects is necessary for successful treatment or is just an unwanted and unnecessary side effect. Based on these concept, a photocoagulation technique was developed to treat the retina selectively (SRT - Selective retinal therapy), with minimal or no damage to the sensory layers. While the treatment is very similar to regular photocoagulation, the SRT laser uses much lower energy and very short pulses. As a result, treatment does not result in visible burns to the retina and previous studies have shown that the sensory layer remains intact. The aim of this study is to determine the effect of SRT on the resolution of the edema.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Macular Edema
Keywords
DME, Laser, Selective laser therapy, photocoagulation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
32 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Laser therapy
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
Nd: YLF laser treatment
Other Intervention Name(s)
SRT
Intervention Description
grid selective retinal treatment
Primary Outcome Measure Information:
Title
progression of macular edema
Description
Proportion progressing to center involved macular edema by month 12 as confirmed on SD-OCT
Time Frame
12months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Best corrected ETDRS visual acuity letter score >=24 (app. 20/320 or better) Definite retinal thickness due to diabetic macular edema by on clinical exam at or within 500 to 3000 microns of the macular center (radius) for which the investigator believes laser photocoagulation is not indicated A thickness equal or less than 315 microns in the central subfield (confirmed by SD-OCT). A thickness of >2 SD of norm in one or more inner or outer subfields on SD-OCT. Maximal focal/grid laser not yet applied (within areas of thickening between 500 and 3000 microns from center of macula, not all microaneurysms treated with direct laser and not all other areas of thickening treated with grid laser). Maximal or complete laser treatment is defined as direct treatment to all microaneurysms within areas of edema and grid treatment to all other areas of macular edema. No panretinal scatter photocoagulation (PRP) within prior 4 months. No recent medical treatment for DME (e.g., intravitreal/peribulbar steroids within past 4 months or intravitreal anti-VEGF injection within past 2 months). No major ocular surgery (including cataract extraction, any other intraocular surgery, scleral buckle, glaucoma filter, cornea transplant, etc.) within prior 6 months. No Nd:YAG laser capsulotomy within prior 2 months. Macular edema is not considered to be due to a cause other than diabetic macular edema o An eye should not be considered eligible (1) if the macular edema is considered to be related to cataract extraction or (2) clinical exam and/or SD-OCT suggests that vitreoretinal interface disease (eg. vitreoretinal traction or epiretinal membrane) is the primary cause of the macular edema. Media clarity, pupillary dilation, and patient cooperation sufficient for adequate fundus photos. No ocular condition (other than diabetes) that, in the opinion of the investigator, might affect macular edema or alter visual acuity during the first 12 months of the study (e.g., vein occlusion, uveitis or other ocular inflammatory disease, neovascular glaucoma, Irvine-Gass Syndrome). Glaucoma per se is not an exclusion Exclusion Criteria: History of renal failure requiring dialysis or renal transplant Condition that in the opinion of the investigator would preclude participation in the study (e.g., unstable medical status including blood pressure and glycemic control) Patients in poor glycemic control who recently (>3 months) initiated intensive insulin treatment (a pump or multiple daily injections) or plan to do so in the next 3 months should not be enrolled. A patient with only one functioning eye (i.e., letter score 0 in contra-lateral eye)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anat Loewenstein, MD
Organizational Affiliation
Tel-Aviv Sourasky Medical Center
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Joseph Moisseiev, Prof.
Organizational Affiliation
Sheba Medical Center
Official's Role
Study Director
Facility Information:
Facility Name
Tel Aviv Sourasky Medical Center
City
Tel Aviv
ZIP/Postal Code
64329
Country
Israel
Facility Name
Sheba Medical Center
City
Tel Hahsomer
ZIP/Postal Code
52621
Country
Israel

12. IPD Sharing Statement

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Evaluation of the Effects of Selective Photocoagulation for the Treatment of Diabetic Macular Edema

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