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Impact of the Navilas ® Micropulse Laser Treatment for Macular Edema Within the CHU Brugmann Hospital Macular Edema

Completed
Conditions
Macular Edema
Interventions
Other: Data extraction from medical files
Registration Number
NCT04857099
Lead Sponsor
Brugmann University Hospital
Brief Summary

The Navilas® micropulse laser can be used to treat patients with macular edema and good visual acuity, which therefore do not fall within the indications for conventional treatments by intravitreal injections.

The CHU Brugmann Hospital is the only center to own this laser in Belgium.This study aims to evaluate the efficacy of this laser.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
23
Inclusion Criteria
  • Diffuse macular edema without focal edema source accessible by focal laser (e.g. capillary telangiectasia)
  • Central retinal thickness ≤ 400microns.
  • Patient does not meet the reimbursement criteria for intra-vitreous injections(IVI) of anti-VEGF (eg AV> 5/10).
  • IVI are contraindicated.
  • Physician considers that it is preferable to space out the injections because of the side effects (eg. ocular disturbance during IVI, eye pain, sensation of a foreign body, spots in the visual field generating a visual gene etc.)
  • Patient wishing to space the anti-VEGF IVI.
Exclusion Criteria
  • Macular edema of a different etiology than diabetic macular edema or venous thrombosis (e.g. cataract extraction, vitreomacular traction, epiretinal membrane etc.)
  • Central retinal thickness > 400 microns.
  • The eye presents a focal edematous maculopathy accessible to conventional laser.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Macular edemaData extraction from medical files-
Primary Outcome Measures
NameTimeMethod
Visual acuityBaseline versus three months after treatment
Scar - assessed by fluorescein angiographyThree months after treatment
Periodicity of anti-VEGF injectionsBaseline versus three months after treatment
Scar - assessed by optical coherence tomographyThree months after treatment
Scar - assessed by auto-fluorescence fundus imagesThree months after treatment
Retinal thickness changeBaseline versus three months after treatment
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

CHU Brugmann

🇧🇪

Brussels, Belgium

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