MEM: Sub-threshold Photocoagulation of Diabetic Macular Oedema

Sponsor
Manchester University NHS Foundation Trust (Other)
Overall Status
Withdrawn
CT.gov ID
NCT02309476
Collaborator
Topcon Corporation (Industry), Optos, PLC (Industry)
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Study Details

Study Description

Brief Summary

Topcon's Endpoint Management (EM) is a new software from the Pascal® laser which allows us to decrease the intensity of the burns (invisible burns) showing some landmarks with normal intensity so the investigators can see the area which has been treated. The Pascal® system with EM utilizes 577nm laser wavelength compared to the 532nm laser wavelength which was utilized in previous Pascal® laser studies.

This study aims to demonstrate that 577nm Pascal® with EM has the same efficacy and effectiveness as 532nm Pascal® in the treatment of diabetic macular oedema.

Condition or Disease Intervention/Treatment Phase
  • Device: PASCAL Laser, Green Laser 0.75
  • Device: PASCAL Laser, Green Laser 1
  • Device: PASCAL Laser, 70% Yellow Laser 0.75
  • Device: PASCAL Laser, 70% Yellow Laser 1
  • Device: PASCAL Laser, 40% Yellow Laser 0.75
  • Device: PASCAL Laser, 40% Yellow Laser 1
N/A

Detailed Description

Diabetic macular oedema (DMO) remains the most common cause of visual loss in diabetic patients and affects around 29% of diabetic patients with 20 or more years of disease. The Early Treatment Diabetic Retinopathy Study (ETDRS) demonstrated a significant benefit of laser photocoagulation for the treatment of clinically significant macular oedema, reducing the incidence of vision loss by approximately 50% at 3 years' follow-up.

The original ETDRS photocoagulation technique was adopted throughout the world and gradually modified through the years. Despite the great improvements, loss of central vision, paracentral scotoma and decreased color vision are some adverse events that can still occur, mostly caused by the progressive enlargement of the laser scars consequent to the visible burn of conventional laser photocoagulation.

New strategies have been developed for laser treatments that minimize the chorioretinal damage while maintaining at least similar treatment efficacy.

And numerous clinical studies have been conducted with subvisible laser treatments. However, the lack of a visible endpoint makes it difficult for the treating physician to know which retinal areas have been treated in order to avoid retreatment and also to be confident that the desired target tissue had been treated.

Topcon's Endpoint Management (EM) is a new software from the Pascal® laser which allows us to decrease the intensity of the burns (invisible burns) showing some landmarks with normal intensity so the investigators can see the area which has been treated.

The Pascal® system with EM utilizes 577nm laser wavelength compared to the 532nm laser wavelength which was utilized in previous Pascal® laser studies.

This study aims to demonstrate that 577nm Pascal® with EM has the same efficacy and effectiveness as 532nm Pascal®.

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Manchester Pascal Endpoint Management Laser Treatment of Diffuse Diabetic Macular Oedema (DMO): A Safety and Efficacy Study
Study Start Date :
Oct 1, 2012
Actual Primary Completion Date :
Dec 1, 2014
Anticipated Study Completion Date :
Dec 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: PASCAL Laser, Green Laser 0.75

Barely Visible Pascal laser grid using 532nm "green" wavelength, 0.75 burn-widths-apart. Intervention: macular laser grid Number of burns: Full grid 112 burns Spot size: 100micron Duration: 10 ms Exposure: barely visible burn Average power: 100 to 1000 mW Spot spacing: 0.75 burn-widths-apart Distribution: Grid

Device: PASCAL Laser, Green Laser 0.75
Barely Visible Pascal laser grid using 532nm "green" wavelength, 0.75 burn-widths-apart. Intervention: macular laser grid Number of burns: Full grid 112 burns Spot size: 100micron Duration: 10 ms Exposure: barely visible burn Average power: 100 to 1000 mW Spot spacing: 0.75 burn-widths-apart Distribution: Grid

Experimental: PASCAL Laser, Green Laser 1 burn

Barely Visible Pascal laser grid using 532nm "green" wavelength, 1 burn-widths-apart Intervention: macular laser grid Number of burns: Full grid 112 burns Spot size: 100micron Duration: 10 ms Exposure: barely visible burn Average power: 100 to 1000 mW Spot spacing: 1 burn-widths-apart Distribution: Grid

Device: PASCAL Laser, Green Laser 1
Barely Visible Pascal laser grid using 532nm "green" wavelength, 1 burn-widths-apart. Intervention: macular laser grid Number of burns: Full grid 112 burns Spot size: 100micron Duration: 10 ms Exposure: barely visible burn Average power: 100 to 1000 mW Spot spacing: 0.75 burn-widths-apart Distribution: Grid

Experimental: PASCAL Laser, 70% Yellow Laser 0.75

Pascal EM at 70% 577nm "yellow" laser grid, 0.75 burn-widths-apart Intervention: macular laser grid Number of burns: Full grid 112 burns Spot size: 100micron Duration: 10 ms Exposure: A barely visible burn will be aimed at for the "Landmark" burn and EndPoint Management will be set at 70% to achieve non-visible burns Average power: 100 to 1000 mW Spot spacing: 0.75 burn-widths-apart Distribution: Grid

Device: PASCAL Laser, 70% Yellow Laser 0.75
Pascal EM at 70% 577nm "yellow" laser grid, 0.75 burn-widths-apart Intervention: macular laser grid Number of burns: Full grid 112 burns Spot size: 100micron Duration: 10 ms Exposure: A barely visible burn will be aimed at for the "Landmark" burn and EndPoint Management will be set at 70% to achieve non-visible burns Average power: 100 to 1000 mW Spot spacing: 0.75 burn-widths-apart Distribution: Grid

Experimental: PASCAL Laser, 70% Yellow Laser 1

Pascal EM at 70% 577nm "yellow", 1 burn-widths-apart Intervention: macular laser grid Number of burns: Full grid 112 burns Spot size: 100micron Duration: 10 ms Exposure: A barely visible burn will be aimed at for the "Landmark" burn and EndPoint Management will be set at 70% to achieve non-visible burns Average power: 100 to 1000 mW Spot spacing: 1 burn-widths-apart Distribution: Grid

Device: PASCAL Laser, 70% Yellow Laser 1
Pascal EM at 70% 577nm "yellow" laser grid, 0.75 burn-widths-apart Intervention: macular laser grid Number of burns: Full grid 112 burns Spot size: 100micron Duration: 10 ms Exposure: A barely visible burn will be aimed at for the "Landmark" burn and EndPoint Management will be set at 70% to achieve non-visible burns Average power: 100 to 1000 mW Spot spacing: 1 burn-widths-apart Distribution: Grid

Experimental: PASCAL Laser, 40% Yellow Laser 0.75

Pascal EM at 40% 577nm "yellow", 0.75 burn-widths-apart Intervention: macular laser grid Number of burns: Full grid 112 burns Spot size: 100micron Duration: 10 ms Exposure: A barely visible burn will be aimed at for the "Landmark" burn and EndPoint Management will be set at 40% to achieve non-visible burns Average power: 100 to 1000 mW Spot spacing: 0.75 burn-widths-apart Distribution: Grid

Device: PASCAL Laser, 40% Yellow Laser 0.75
Pascal EM at 40% 577nm "yellow" laser grid, 0.75 burn-widths-apart Intervention: macular laser grid Number of burns: Full grid 112 burns Spot size: 100micron Duration: 10 ms Exposure: A barely visible burn will be aimed at for the "Landmark" burn and EndPoint Management will be set at 740% to achieve non-visible burns Average power: 100 to 1000 mW Spot spacing: 0.75 burn-widths-apart Distribution: Grid

Experimental: PASCAL Laser, 40% Yellow Laser 1

Pascal EM at 40% 577nm "yellow" laser grid, 1 burn-widths-apart Intervention: macular laser grid Number of burns: Full grid 112 burns Spot size: 100micron Duration: 10 ms Exposure: A barely visible burn will be aimed at for the "Landmark" burn and EndPoint Management will be set at 40% to achieve non-visible burns Average power: 100 to 1000 mW Spot spacing: 1 burn-widths-apart Distribution: Grid

Device: PASCAL Laser, 40% Yellow Laser 1
Pascal EM at 40% 577nm "yellow" laser grid, 0.75 burn-widths-apart Intervention: macular laser grid Number of burns: Full grid 112 burns Spot size: 100micron Duration: 10 ms Exposure: A barely visible burn will be aimed at for the "Landmark" burn and EndPoint Management will be set at 740% to achieve non-visible burns Average power: 100 to 1000 mW Spot spacing: 0.75 burn-widths-apart Distribution: Grid

Outcome Measures

Primary Outcome Measures

  1. reduction of diabetic macular edema (central retinal thickness) within the 6 arms of the study [12 months]

    To compare Green Pascal® laser and Yellow Pascal® laser using EM among 6 groups of participants using Pascal® laser with an application of full grid 112 burns in a single session

Secondary Outcome Measures

  1. Improvement in visual acuity (> 10 letters or two lines in the ETDRS chart) [12 months]

  2. increase in retinal sensitivity within the 6 arms of the study [12 months]

    increase in retinal sensitivity will be assessed with fundus-related perimetry (microperimetry)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Patient-eligibility

Inclusion criteria:
  1. Older than 18 years of age

  2. Male or female patients with diabetes mellitus type I or type 2 who meet the WHO or ADA criteria for diabetes

  3. Able to give informed consent

Study Eye eligibility

Inclusion criteria:
  1. ETDRS visual acuity equivalent to 35 letters or better (Snellen equivalent 20/200 or better)

  2. The patient must have non-proliferative diabetic retinopathy (NPDR) with diffuse macular oedema

  3. Mean average central retinal thickness at least 300 microns as measured by Deep Range Imaging Optical Coherence Tomography (DRI -OCT) scans

  4. Adequate pupil dilatation and clear media to perform wide-field colour, red-free imaging and fundus fluorescein angiography (WF-FFA), wide-field fundus autofluorescence imaging (WF-AF) and DRI-OCT

  5. Ability to perform accurate Humphmrey visual field test

Exclusion Criteria:

Patient-eligibility

Exclusion criteria:
  1. History of chronic renal failure or renal transplant for diabetic nephropathy

  2. Recent (last 6 months) or on-going poor glycaemic control. H1Ac greater than 10.0mg/dL

  3. Creatinine greater than 1.2 mg/dL

  4. HDL equal to or greater than 40 mg/dL

  5. Uncontrolled hypertension. Blood pressure greater or equal to 180/110 mmHg

  6. Patient is unavailable for follow-up visits

  7. Pregnant women or breast-feeding females

Study Eye eligibility

Exclusion criteria:
  1. Lens opacity that could influence vision and results

  2. Proliferative Diabetic Retinopathy.

  3. Any surgical or non-retinal laser treatment to the study eye within 2 months

  4. Narrow drainage angles with raised intraocular pressure and angle closure glaucoma.

  5. Planned YAG peripheral iridotomy

  6. Previous retinal laser photocoagulation, intraocular drug therapy, or macular laser treatment to treatment eye in last year

  7. Vitreomacular traction determined clinically and / or OCT, which in the opinion of the investigator, contributes to macular edema (associated or cause a detachment of the fovea) and prevents the improvement with treatment.

  8. Atrophy / scar / fibrosis involving the center of the macula, including evidence of atrophy treated with laser within 200 microns of the FAZ.

  9. Any previous ocular condition that may be associated with a risk of macular edema

  10. Important known allergies to sodium fluorescein dye used in angiography.

  11. Active lid or adnexal infection 13. Planned intra-ocular surgery within one year

Contacts and Locations

Locations

Site City State Country Postal Code
1 Central Manchester Foundation Trust Manchester England United Kingdom M13 9WL

Sponsors and Collaborators

  • Manchester University NHS Foundation Trust
  • Topcon Corporation
  • Optos, PLC

Investigators

  • Principal Investigator: Paulo Stanga, Manchester Royal Eye Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Emma Columbine, Professor Paulo Stanga, Manchester University NHS Foundation Trust
ClinicalTrials.gov Identifier:
NCT02309476
Other Study ID Numbers:
  • R03018
First Posted:
Dec 5, 2014
Last Update Posted:
Mar 17, 2020
Last Verified:
Mar 1, 2020
Keywords provided by Emma Columbine, Professor Paulo Stanga, Manchester University NHS Foundation Trust
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 17, 2020