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CompletedNCT00442156Laser RespUpdated Aug 26, 2016

The Course of Response to Focal Photocoagulation for DME

An observational study in Diabetic Retinopathy and Diabetic Macular Edema, sponsored by Jaeb Center for Health Research. Completed at 32 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2016-08-26.

Sponsored by Jaeb Center for Health Research · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
122
Ages
18 Years and older
Sex
All
01

Study summary

The study objective is to determine the course of changes in OCT measured macular thickness and visual acuity following a single session of focal photocoagulation for center-involved DME. The response will be evaluated separately in eyes with and without prior focal photocoagulation for DME. The purpose is to determine the proportion of eyes that continue to improve at least 5 letters in visual acuity or at least 10% in central retinal thickness after a session of focal photocoagulation. In addition, the study will explore whether any baseline factors can be identified that are predictive of the response.

All subjects will have follow-up visits 8 weeks and 16 weeks post treatment. At the 16-week visit, study eyes are evaluated for change in retinal thickness and visual acuity from baseline.

  • Treatment is to be deferred and follow up continued if visual acuity letter score has improved by >5 or OCT central subfield thickness has decreased by >10% compared with baseline.
  • If visual acuity letter score has not improved by at least 5 and OCT central subfield thickness has not decreased by at least 10%, then the eye is classified as 'not improved' and the investigator may provide additional treatment. Follow up ends for eyes that receive additional treatment at this visit. However, if the investigator and participant elect to defer additional treatment (even if deferral criteria are not met), then follow up will continue until the study eye receives additional treatment for DME.
  • Eyes continuing in follow up have visits every 8 weeks (+1week) as long as there has been continued improvement in visual acuity (letter score improved >5 ) or retinal thickness (central subfield thickness decreased by >10%) compared with the visit 16 weeks earlier. The longest follow-up time will be 48 weeks.

By providing information on the length of time during which clinically meaningful improvement occurs following focal photocoagulation, clinicians will be better able to determine when further photocoagulation or other treatments should be considered for persistent DME. Depending on the results of this study, a future randomized clinical trial will be considered comparing the more aggressive retreatment photocoagulation regimen currently serving as the standard DRCR Network approach to focal photocoagulation for macular edema with the less aggressive regimen evaluated in this protocol.

Read the detailed description

Focal photocoagulation is the only treatment that has been demonstrated to be beneficial for diabetic macular edema. In the ETDRS, focal photocoagulation of eyes with macular edema reduced the risk of moderate visual loss (decrease of 15 or more letters) by approximately 50% (from 24% to 12%, three years after initiation of treatment). For eyes with center-involved DME and visual acuity worse than 20/40 that were treated with focal photocoagulation, the 15-letter improvement rate at 1 year was 11% and at 3 years was 16%.

In the ETDRS, focal photocoagulation treatment for diabetic macular edema involved direct treatment to discrete lesions between 500 microns and 3000 microns from the center of the macula that were thought to be causing retinal thickening or hard exudates with or without "grid" treatment to other macular areas of retinal thickening or non-perfusion. The lesions treated directly included microaneurysms, identified on fluorescein angiography, that either filled or leaked, intraretinal microvascular abnormalities (IRMA), or pruned capillaries that leaked fluorescein. Grid treatment was applied in the ETDRS to areas of thickened retina that showed diffuse fluorescein leakage or areas of non-perfusion identified as capillary dropout on fluorescein angiography. Areas of non-perfusion in the macula could be treated with grid at the discretion of the treating ophthalmologist. Areas that had both discrete lesions and diffuse leakage or capillary dropout would receive a combination of direct and grid treatment. Re-treatment was applied at four month intervals if clinically significant macular edema persisted, one or more treatable lesions were identified, and the investigator believed these lesions were responsible for the edema. The median number of focal laser treatments applied in the ETDRS was 3.8.

The mechanism of action of focal photocoagulation is not fully understood; however, it is clear that the retinal pigment epithelium (RPE) absorbs the majority of the laser energy and thermal injury occurs at the level of the RPE. Studies have shown that photocoagulation can eventually result in retinal and apparent RPE atrophy 200-300% larger than the original laser spot size. These areas of expanded atrophy can lead to loss of central vision, central scotomata, and decreased color vision. Consequently, many retinal specialists today tend to treat with lighter, less intense laser burns than originally specified in the ETDRS.

In addition to the concern regarding the spread of intense laser burns, there are a number of other reasons that retinal specialists today have modified the treatment procedures originally specified in the ETDRS protocol. These reasons include the advent of new lasers and the clinical observation that different techniques, such as focal photocoagulation with lighter burns or grid treatment alone, may be similar in beneficial effect as the original ETDRS treatment protocol. A modified ETDRS focal photocoagulation protocol adapted from the original ETDRS approach, has been adopted as the standard laser technique for DME used in DRCRnet studies.

There are limited data on the course of visual acuity and central retinal thickness after a single focal photocoagulation session for DME. In prior DRCRnet DME treatment protocols that included a laser arm, according to the re-treatment protocol eyes received a second focal photocoagulation session at 3.5- 4 months (which was the first follow-up visit) unless there was substantial improvement defined as at least a 50% decrease in retinal thickening of the central subfield measurement on OCT. As a result, it is unknown what proportion of eyes with lesser degrees of improvement would have continued to improve and the time course for further improvement following the initial photocoagulation session given additional time. In one study conducted by DRCRnet of eyes that had not been previously treated for DME, among 113 eyes in the modified ETDRS laser treatment group with baseline OCT central subfield >250 microns, a 50% or more reduction in OCT central subfield thickening was present at 3.5 months in only 28 (25%). The table below categorizes the 85 eyes that did not meet this measure of improvement at 3.5 months with regard to improvement in visual acuity of at least 5 letters and/or reduction in central subfield thickness of at least 10%. The 5 letter reduction was selected based on the 95% confidence interval for change determined in a study that evaluated the validity and reliability of the electronic ETDRS visual acuity testing procedure that is used in DRCRnet protocols. The 10% threshold was selected based on the DRCRnet OCT reproducibility study which found that a 10% change in central subfield thickness was likely to be real. Forty-seven (42%) eyes that met the protocol requirement for repeat photocoagulation at the first follow-up visit had an improvement in either visual acuity (of at least 5 letters), central subfield (of at least a 10% reduction), or both at this follow-up visit.

Other DRCRnet protocols provide data on the course following a single photocoagulation session through 4 months of follow up. In a pilot study designed to evaluate peribulbar corticosteroids for mild DME (OCT central subfield thickness = 250 microns and visual acuity 20/40 or better at baseline), modified ETDRS focal photocoagulation was the treatment given to the control group. Follow-up visits occurred after 1, 2, and 4 months before the eye was eligible to be retreated. Twenty-one of the 37 eyes in the laser group had not been previously treated with focal photocoagulation for DME and 17 eyes had been previously treated with focal photocoagulation. A 50% or more reduction in OCT central subfield thickening occurred in 11 (30%) of the 37 eyes at 17 weeks. Fourteen (38%) eyes that would have met the criteria for re-treatment had an improvement in either visual acuity (of at least 5 letters), central subfield (of at least 10%), or both at 17 weeks.

In another pilot study evaluating intravitreal bevacizumab for DME (OCT central subfield thickness = 275 microns and visual acuity 20/32 or worse at baseline), modified ETDRS focal photocoagulation was the treatment given to the control group. Follow-up visits occurred after 3, 6, 9, and 12 weeks before the eye was eligible to be retreated. There were 7 eyes in the laser group that had not been previously treated with focal photocoagulation for DME and 12 eyes that had been previously treated with focal photocoagulation. Among these 19 eyes, a 50% or more reduction in OCT central subfield thickening occurred in 3 (16%) at 12 weeks. Ten (53%) eyes that would have met criteria for re-treatment had an improvement in either visual acuity (of at least 5 letters), central subfield (of at least 10%), or both at 12 weeks.

The data from these three protocols indicate that a substantial number of eyes receiving focal photocoagulation (either an initial course or repeat application) will show improvement in central retinal thickness after 3-4 months that is at least 10% but is less than 50% of the baseline thickening. It is for these eyes that further knowledge of the course of retinal thickening and visual acuity without additional interventions is needed to assess whether the present requirements for re-treatment are more aggressive than they need to be.

02

Conditions studied

  • Diabetic Retinopathy
  • Diabetic Macular Edema

Keywords

  • Laser photocoagulation
03

In context

Macular Edema

841 studies on the registry are indexed under Macular Edema; 56 are open to participants now.

This study's enrollment of 122 is above the median of 97 across 163 observational studies indexed under Macular Edema.

Browse Macular Edema studies →

Lead sponsor

Jaeb Center for Health Research is the lead sponsor of 126 studies on the registry; 17 are open to participants now.

Of its 16 completed or terminated interventional studies of FDA-regulated products, 14 (88%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Diabetics within the United States who are at least 18 years old and have DME treatable with laser photocoagulation.

Inclusion criteria

To be eligible, the following inclusion criteria must be met:

  • Age >= 18 years
  • Diagnosis of diabetes mellitus (type 1 or type 2.
  • At least one eye meets the study eye criteria.
  • Able and willing to provide informed consent.

The subject must have one eye meeting all of the inclusion criteria and none of the exclusion criteria listed below. If both eyes are eligible, the study eye is selected by the investigator and subject.

  • Best corrected E-ETDRS visual acuity letter score >= 24 (i.e., 20/320 or better) within 8 days of enrollment.
  • On clinical exam, definite retinal thickening due to diabetic macular edema involving the center of the macula.
  • OCT central subfield >=250 microns within 8 days of enrollment.
  • Media clarity, pupillary dilation, and subject cooperation sufficient for adequate OCT.
  • Investigator believes that focal photocoagulation is the most appropriate treatment for the DME.
  • Study Eye Exclusion Criteria

Exclusion criteria

Exclusion Criteria

A subject is not eligible if any of the following exclusion criteria are present:

  • Significant renal disease, defined as a history of chronic renal failure requiring dialysis or kidney transplant.
  • A condition that, in the opinion of the investigator, would preclude participation in the study (e.g., unstable medical status including blood pressure, cardiovascular disease, and glycemic control).
  • Blood pressure > 180/110 (systolic above 180 OR diastolic above 110).
  • Participation in an investigational trial within 30 days of enrollment that involved treatment with any drug that has not received regulatory approval at the time of study entry.
  • Subject is expecting to move out of the area of the clinical center to an area not covered by another clinical center during the next 6 months.

The following exclusions apply to the study eye only (i.e., they may be present for the nonstudy eye):

  • Macular edema is considered to be due to a cause other than diabetic macular edema.
  • An ocular condition is present such that, in the opinion of the investigator, visual acuity loss would not improve from resolution of macular edema (e.g., foveal atrophy, pigment abnormalities, dense subfoveal hard exudates, significant macular ischemia, nonretinal condition).
  • An ocular condition is present (other than diabetes) that, in the opinion of the investigator, might affect macular edema or alter visual acuity during the course of the study (e.g., vein occlusion, uveitis or other ocular inflammatory disease, neovascular glaucoma, etc.).
  • Substantial cataract that, in the opinion of the investigator, is likely to be decreasing visual acuity by 3 lines or more (i.e., cataract would be reducing acuity to 20/40 or worse if eye was otherwise normal).
  • History of treatment for DME at any time in the past 4 months (such as focal/grid macular photocoagulation, intravitreal or peribulbar corticosteroids, anti-VEGF drugs, or any other treatment).
  • History of panretinal (scatter) photocoagulation (PRP) within 4 months prior to enrollment or anticipated to be performed within next 6 months.
  • History of major ocular surgery (including vitrectomy, cataract extraction, scleral buckle, any intraocular surgery, etc.) within prior 4 months or anticipated within the next 6 months.
  • History of YAG capsulotomy performed within 2 months prior to enrollment
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
122 participants (actual)

Groups and cohorts

  • Laser

    People with diabetic macular edema involving the center of the macula (OCT central subfield thickness \>250 microns), who were already intended to receive focal photocoagulation

    Procedure: Laser photocoagulation

Interventions

  • ProcedureLaser photocoagulation

    modified ETDRS focal photocoagulation generally completed in a single sitting on the day of enrollment, but if little or no improvement, may be repeated at 16 weeks

    Also known as: Laser

06

What researchers measure

Primary outcomes

  1. OCT-measured retinal thickness and visual acuity

    Time frame: 16 weeks

07

Study locations

32 sites
  • Southern California Desert Retina Consultants, MC
    Palm Springs, California 92262, United States
  • Retina Consultants of Southwest Florida
    Fort Myers, Florida 33912, United States
  • Retina Vitreous Consultants
    Ft. Lauderdale, Florida 33484, United States
  • Central Florida Retina Institute
    Lakeland, Florida 33805, United States
  • Southeast Retina Center, P.C.
    Augusta, Georgia 30909, United States
  • Retina Associates of Hawaii, Inc.
    Honolulu, Hawaii 96813, United States
  • Raj K. Maturi, M.D., P.C.
    Indianapolis, Indiana 46290, United States
  • American Eye Institute
    New Albany, Indiana 47150, United States
  • Retina and Vitreous Associates of Kentucky
    Lexington, Kentucky 40509, United States
  • Paducah Retinal Center
    Paducah, Kentucky 42001, United States
  • Maine Vitreoretinal Consultants
    Bangor, Maine 04401, United States
  • Elman Retina Group, P.A.
    Baltimore, Maryland 21237, United States
  • Southern New England Retina Associates
    Attleboro, Massachusetts 02703, United States
  • Ophthalmic Consultants of Boston
    Boston, Massachusetts 02114, United States
  • Joslin Diabetes Center
    Boston, Massachusetts 02215, United States
  • Vitreo-Retinal Associates
    Grand Rapids, Michigan 49525, United States
  • Associated Retina Consultants
    Williamsburg, Michigan 49690, United States
  • Delaware Valley Retina Associates
    Lawrenceville, New Jersey 08648, United States
  • University of Rochester
    Rochester, New York 14642, United States
  • Retina-Vitreous Surgeons of Central New York, PC
    Syracuse, New York 13224, United States
  • University of North Carolina, Dept. of Ophthalmology
    Chapel Hill, North Carolina 27599, United States
  • Charlotte Eye, Ear, Nose and Throat Assoc., PA
    Charlotte, North Carolina 28210, United States
  • Retina Associates of Cleveland, Inc.
    Beachwood, Ohio 44122, United States
  • Casey Eye Institute
    Portland, Oregon 97239, United States
  • Palmetto Retina Center
    Columbia, South Carolina 29169, United States
  • Carolina Retina Center
    Columbia, South Carolina 29223, United States
  • Retina Research Center
    Austin, Texas 78705, United States
  • Texas Retina Associates
    Dallas, Texas 75231, United States
  • Charles A. Garcia, PA & Associates
    Houston, Texas 77002, United States
  • Retina and Vitreous of Texas
    Houston, Texas 77025, United States
  • Texas Retina Associates
    Lubbock, Texas 79424, United States
  • University of Wisconsin-Madison, Dept. of Ophthalmology
    Madison, Wisconsin 53705, United States
08

References and documents

Publications

  • Diabetic Retinopathy Clinical Research Network. The course of response to focal/grid photocoagulation for diabetic macular edema. Retina. 2009 Nov-Dec;29(10):1436-43. doi: 10.1097/IAE.0b013e3181bcef6b. PubMed 19898182 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 26, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00442156
Lead sponsor
Jaeb Center for Health Research
Collaborators
National Eye Institute (NEI)
First posted
Mar 1, 2007
Start date
Jan 2007
Primary completion
Jun 2008
Completion
Jun 2008
Last update
Aug 26, 2016

Study contacts

David Browning, M.D.
study chair · Charlotte Eye, Ear, Nose and Throat Assoc., PA

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2016. You cannot join it, but the record below documents what was studied.

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