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
Group Intervention Description Macular edema Data extraction from medical files -
- Primary Outcome Measures
Name Time Method Visual acuity Baseline versus three months after treatment Scar - assessed by fluorescein angiography Three months after treatment Periodicity of anti-VEGF injections Baseline versus three months after treatment Scar - assessed by optical coherence tomography Three months after treatment Scar - assessed by auto-fluorescence fundus images Three months after treatment Retinal thickness change Baseline versus three months after treatment
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
CHU Brugmann
🇧🇪Brussels, Belgium