Brief Title
Effects of OCTA-guided PDT in Acute CSC
Official Title
Effects of Optical Coherence Tomography Angiography-guided Photodynamic Therapy in Acute Central Serous Chorioretinopathy
Brief Summary
OCTA-guided PDT is as safe and effective as ICGA-guided PDT in the treatment of acute central serous chorioretinopathy. Or OCTA-guided PDT is more effective than ICGA-guided PDT in the treatment of acute central serous chorioretinopathy, safe as well.
Study Type
Interventional
Primary Outcome
Number of patients with subretinal fluid resolution on OCT after PDT of two groups
Secondary Outcome
Number of patients with leakage point resolution on FFA after PDT of two groups
Condition
Central Serous Chorioretinopathy
Intervention
OCTA-guided Photodynamic therapy
Study Arms / Comparison Groups
OCTA group
Description: Patients in this group underwent OCTA-guided half-dose photodynamic therapy.
Publications
* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
Recruitment Information
Recruitment Status
Procedure
Estimated Enrollment
23
Start Date
September 1, 2017
Completion Date
March 27, 2018
Primary Completion Date
December 1, 2017
Eligibility Criteria
Inclusion Criteria: - Idiopathic detachment of the neurosensory retina with a focal leak at the level of the RPE with FA - Presence of SRF and/or serous pigment epithelial detachment on OCT - Presence of abnormal dilated choroidal vasculature in ICGA Exclusion Criteria: - Patients with other ocular conditions commonly associated with SRF, such as choroidal neovascularization, polypoidal choroidal vasculopathy (PCV), diabetic retinopathy, retinal vascular occlusion, Coat's disease - Any disease that may affect the quality of imaging (quality of OCTA images < 6), such as cataract, high myopia or nystagmus - History of ocular surgeries including retinal laser - Pregnancy - Any uncontrolled systemic disease - Any condition rendering patients intolerable to image acquisition
Gender
All
Ages
18 Years - 65 Years
Accepts Healthy Volunteers
No
Contacts
Mingwei Zhao, M.D, ,
Location Countries
China
Location Countries
China
Administrative Informations
NCT ID
NCT03497000
Organization ID
Peking UPH
Responsible Party
Principal Investigator
Study Sponsor
Peking University People's Hospital
Collaborators
National Natural Science Foundation of China
Study Sponsor
Mingwei Zhao, M.D, Study Director, Peking University People's Hospital
Verification Date
April 2018