Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
270 participants
INTERVENTIONAL
2019-02-12
2024-12-11
Brief Summary
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Detailed Description
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Acts which are the subject of the study: indocyanine green-Guided Targeted Laser photocoagulation (IGTL): this combines routine procedures, that are, the detection of macro-aneurysms by ICG angiography, laser photocoagulation and optional post-laser verification of the effectiveness of the photothrombosis by OCT.
Study act: the treatment study includes a baseline laser treatment (experimental group) or sham laser (control group) at randomization, repeated if needed 3 month later, administered in combination with anti VEGF treatment, consisting of 3 monthly injections in the first 3 months, and a maintenance phase with monthly visits where retreatment is administered as needed through a PRN regimen, based on morphological (retinal thickness on OCT) and functional (visual acuity) criteria.
To evaluate the interest of IGTL in real conditions, the choice of the anti VEGF treatment used for intravitreal injection (Ranibizumab or Aflibercept, which have French marketing authorizations) is left to each investigator (equivalent therapeutic efficacy). Bevacizumab is ruled out due to its lower efficacy compared with Aflibercept among eyes with worse baseline VA, that represent the majority of the patients in our study. In addition, bevacizumab is currently off-label in France for DME If both eyes are eligible at the time of randomization, only one eye will be included and analyzed. However, the fellow eye will be treated with the randomization-assigned treatment and the testing will be performed on each eye.
Risks and constraints involved in the study: these procedures are commonly done in ophthalmology care settings; no additional risk is expected due to the study.
Expected benefits for the participants and for the company: These procedures are commonly done in ophthalmology care settings; no additional risk is expected due to the study.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
Both group with laser or sham laser will be performed in combination with anti VEGF treatment
PREVENTION
DOUBLE
Study Groups
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Experimental Group
Indocyanine green-Guided Targeted Laser photocoagulation combines routine procedures, that are, the detection of macro-aneurysms by ICG angiography, laser photocoagulation and optional post-laser verification of the effectiveness of the photothrombosis by OCT. Indocyanine green-Guided Targeted Laser photocoagulation is administered in combination with anti VEGF treatment
Indocyanine green-Guided Targeted Laser photocoagulation
Detection of macro-aneurysms by ICG angiography, laser photocoagulation and optional post-laser verification of the effectiveness of the photothrombosis by OCT.
Control Group
Sham laser is administered at randomization visit and repeated if needed 3 month later in combination with anti VEGF treatment
Sham laser
Therapeutic procedure used in ophthalmology
Interventions
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Indocyanine green-Guided Targeted Laser photocoagulation
Detection of macro-aneurysms by ICG angiography, laser photocoagulation and optional post-laser verification of the effectiveness of the photothrombosis by OCT.
Sham laser
Therapeutic procedure used in ophthalmology
Eligibility Criteria
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Inclusion Criteria
* with visual acuity lower or equal than 20/32 ( ≤ 74 TaLaDME protocol\_v1.2\_12.07.2018 9/76 ETDRS letters)
* with central retinal thickness of more than 300μm in Spectral Domain OCT (SD-OCT) and/or presence of retro-foveal hard exudates
* due to DME
* with one or more macro-aneurysms with a diameter greater than 150 μm in the posterior pole
* with health insurance
* who signed the written informed consent form
Exclusion Criteria
* Significant opacity of the ocular media that could contribute to decreased visual acuity
* macro-aneurysm(s) mainly responsible for the DME located less than 500μm from the center of the fovea (i.e. within 1 disc radius of the fovea),
* Steroids injection within the last 4 months
* proliferative diabetic retinopathy requiring panretinal photocoagulation or associated with posterior tractional retinal detachment that may be worsened by the use of anti-VEGF therapy
* myocardial infarction or stroke within the last 3 months
* Cataract surgery within the last 3 months
* Local treatment with prostaglandin
* Women who are pregnant, breast feeding or of child bearing age without effective contraception
18 Years
ALL
No
Sponsors
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Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts
OTHER
Responsible Party
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Principal Investigators
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Michel PAQUES, PU-PH
Role: PRINCIPAL_INVESTIGATOR
Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts
Locations
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Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts
Paris, , France
Countries
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References
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Dupas B, Castro-Farias D, Girmens JF, Eginay A, Couturier A, Villeroy F, Delyfer MN, Creuzot-Garcher C, Giocanti-Auregan A, Beral L, Arndt C, Mesnard C, Vicaut E, Chaumet-Riffaud P, Durand-Zaleski I, Paques M. Photocoagulation or sham laser in addition to conventional anti-VEGF therapy in macular edema associated with TelCaps due to diabetic macular edema or retinal vein occlusion (TalaDME): a study protocol for a multicentric, French, two-group, non-commercial, active-control, observer-masked, non-inferiority, randomized controlled clinical trial. Trials. 2024 Apr 22;25(1):273. doi: 10.1186/s13063-024-07994-1.
Other Identifiers
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P18-01
Identifier Type: -
Identifier Source: org_study_id
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