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Subthreshold laser treatment with Endpoint Management in posterior pole diseases associated with sub- and intraretinal fluid.

Subthreshold laser treatment with Endpoint Management in posterior pole diseases associated with sub- and intraretinal fluid.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00015437
Enrollment
50
Registered
2018-09-05
Start date
2018-09-07
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

H35.7

Interventions

Group 1: Subthreshold laser treatment with Endpoint Management. As treatment can be repeated every 3, a maximum of 4 laser treatments can be applied during the 12 months period. Every study patient is

Sponsors

Augenklinik der Ludwig-Maximilians Universität München
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age =18 years, ability to give consent must be given, ability to participate in studies on a regular basis must be given, BCVA better than 0,05, Diagnosis of optic disc pit maculopathy, exsudative choroidal naevus, MacTel type 2 or persistent subretinal fluid after retinal detachment surgery (vitrectomy or buckling) confirmed by retinal specialist, Normal findings in the medical history unless the investigator considers an abnormality to be clinically irrelevant

Exclusion criteria

Exclusion criteria: Any other macular disease with possibility of developing subretinal fluid: vitreomacular traction syndrome, epiretinal membranes, age-related macular degeneration, diabetic retinopathy, choroidal neovascularization, uveitis, Ocular surgery for 3 months preceding the study, Previous intravitreal injections of anti-VEGF, steroids within 3 months preceding the study, Previous macular laser treatment or photodynamic therapy within 6 months preceding the study, Present ocular infection or clinically significant inflammation, Kidney failure or dialysis, Women: Pregnancy or currently breast-feeding ,Allergy to fluorescein, History of systemic or topical corticosteroid use within last 6 months, Patient is not able to cooperate or has any other medical or psychological condition that prohibits him from regular follow-up, Planned intraocular surgery within 12 months

Design outcomes

Primary

MeasureTime frame
Reduction of central subretinal fluid as measured by the decrease in central retinal thickness after 6 months (spectral-domain optical coherence tomography, SD-OCT) .

Secondary

MeasureTime frame
Change in visual acuity (best corrected visual acuity measured by ETDRS letters), Change in retinal sensitivity as measured by microperimetry, Change in Ellipsoid-Zone Defect as measured by En-face-OCT after 12 months

Countries

Germany

Contacts

Public ContactBenedikt Schworm

Augenklinik der Ludwig-Maximilians-Universität München

benedikt.schworm at med.uni-muenchen.de08944001683728

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026