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Subthreshold laser treatment with Endpoint Management in central serous chorioretinopathy

Subthreshold laser treatment with Endpoint Management in central serous chorioretinopathy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00014299
Enrollment
50
Registered
2018-04-05
Start date
2018-04-05
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, treatment can be repeated up to every 3 months. Study visits take place at baseline and at months 1, 2, 3, 6, 9, 12 and include the foll

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 BCVA better than 0,05 Subject is generally healthy and able to give informed consent. Diagnosis of CRCS 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 6 months preceding the study Previous intravitreal injections of anti-VEGF, steroids within 6 months preceding the study Previous macular laser treatment or photodynamic therapy within 3 months preceding the study Present ocular infection or clinically significant inflammation Patient is not able to cooperate or has any other medical or psychological condition that prohibits him from regular follow-up Kidney failure or dialysis Allergy to fluorescein Participation in a clinical trial in the 30 days preceding the study Planned intraocular surgery within one 12 months Women: Pregnancy or currently breast-feeding History of systemic or topical corticosteroid use within last 6 months

Design outcomes

Primary

MeasureTime frame
Average reduction of central retinal thickness as measured by spectral domain optical coherence tomography (SD OCT) after 6 months

Secondary

MeasureTime frame
Change in Visual acuity ("Early Treatment of Diabetic Retinopathy Study"- charts, best corrected visual acuity), Macular function (MAIA® microperimetry) and central choroidal thickness (spectraldomain optical coherence tomography) after 6 and 12 months. Rate of total subretinal fluid resorption and recurrence rate after 6 and 12 months.

Countries

Germany

Contacts

Public ContactBenedikt Schworm

Augenklinik der Ludwig-Maximilians Universität München

benedikt.schworm@med.uni-muenchen.de08944001683728

Outcome results

None listed

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