Trials / Unknown
UnknownNCT05687422
Two Patterns of Micropulse Laser in the Treatment of Chronic Central Serous Chorioretinopathy
A Randomized Controlled Study of Two Patterns of Micropulse Laser in the Treatment of Chronic Central Serous Chorioretinopathy
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- Sponsor
- Beijing Hospital · Other Government
- Sex
- All
- Age
- 18 Years – 50 Years
- Healthy volunteers
- Not accepted
Summary
Central serous chorioretinopathy (CSC) is a common eye disease mainly involving the macular area, causing central visual acuity loss. Recently, subthreshold micropulse laser used in treating chronic CSC is proved to be safe and effective. However, some studies indicate that it's less effective than half dose photodynamic therapy (PDT). Certain physicians, including us, think that this may be related to micropulse laser parameters. Thus we need to explore better laser patterns to replace PDT in treating chronic CSC. The aim of this study is to compare the treatment effect of two different patterns of laser parameters (small and regular spot diameter) in treating chronic CSC. In this randomized, double blinded, controlled trial, by comparing the subretinal fluid regression ratio, central retinal thickness, macular microvisual field, macular vascular density, chroidal volume changes and visual acuity of two groups 6 months after micropulse laser treatment, we aim to evaluate the safety and efficacy of refined micropulse laser in treating chronic CSC.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | 100μm laser spot diameter micropulse laser | 100μm laser spot diameter micropulse laser at baseline, then follow-up for 6 months |
| PROCEDURE | 200μm laser spot diameter micropulse laser | 200μm laser spot diameter micropulse laser at baseline, then follow-up for 6 months |
Timeline
- Start date
- 2023-02-01
- Primary completion
- 2023-12-31
- Completion
- 2023-12-31
- First posted
- 2023-01-18
- Last updated
- 2023-01-18
Source: ClinicalTrials.gov record NCT05687422. Inclusion in this directory is not an endorsement.