Combination of Micropulse Laser With or Without Photodynamic Therapy for Chronic Central Serous Chorioretinopathy
NCT ID: NCT06468540
Last Updated: 2024-06-21
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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NOT_YET_RECRUITING
60 participants
OBSERVATIONAL
2024-06-15
2025-12-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* The patient diagnosed with chronic central serous chorioretinopathy with a history of more than 6 months. The diagnostic criteria for chronic CSC were as follows: FFA examination showed leakage of strong fluorescent spots with the extension of angiography time, and late fluorescence accumulation, accompanied by decreased central vision, darkening of vision, and deformable microopia. Fundus examination showed superficial detachment of retinal neuroepithelium in macula.
* Patients received single micropulse laser therapy or micropulse laser combined with drug-free photodynamic therapy, and had not received other laser or surgical treatment in the six months prior to treatment.
* Patients had follow-up data before and after treatment for 1 month and at least 6 months.
Exclusion Criteria
* During treatment, other treatments other than micropulse laser or drug-free photodynamic therapy were received.
* Various reasons led to incomplete patient data.
18 Years
70 Years
ALL
No
Sponsors
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Beijing Hospital
OTHER_GOV
Responsible Party
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Other Identifiers
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IIT-2024-04-376
Identifier Type: -
Identifier Source: org_study_id
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