Selective Retina Therapy With Real-Time Feedback-Controlled Dosimetry for Treating Acute Idiopathic Central Serous Chorioretinopathy in Korean Patients
Primary Purpose
Central Serous Chorioretinopathy
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Selective retina therapy
Sponsored by
About this trial
This is an interventional treatment trial for Central Serous Chorioretinopathy
Eligibility Criteria
Inclusion Criteria:
- Patients diagnosed with treatment-naïve idiopathic central serous chorioretinopathy
Exclusion Criteria:
- age > 55 years,
- Clinical or angiographic features suggestive of choroidal neovascularization
- Optical coherence tomography findings suggestive of type 1 neovascularization or polypoidal choroidal vasculopathy (e.g., double layer sign or fibrovascular pigment epithelial detachment).
- History of macular laser photocoagulation, photodynamic therapy, or anti-vascular-endothelial growth factor therapy.
- History of exogenous corticosteroid treatment for a systemic disease (e.g., Cushing's syndrome or renal disease).
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Treatment arm
Arm Description
Patients received selective retina therapy
Outcomes
Primary Outcome Measures
Subretinal fluid
Presence or absence of subretinal fluid which identified based on optical coherence tomography images.
Secondary Outcome Measures
Visual acuity
Changes in logarithm of minimal angle of resolution visual acuity during the follow-up, which measured using visual acuity chart.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03339856
Brief Title
Selective Retina Therapy With Real-Time Feedback-Controlled Dosimetry for Treating Acute Idiopathic Central Serous Chorioretinopathy in Korean Patients
Official Title
Selective Retina Therapy With Real-Time Feedback-Controlled Dosimetry for Treating Acute Idiopathic Central Serous Chorioretinopathy in Korean Patients
Study Type
Interventional
2. Study Status
Record Verification Date
November 2017
Overall Recruitment Status
Completed
Study Start Date
January 1, 2017 (Actual)
Primary Completion Date
September 1, 2017 (Actual)
Study Completion Date
October 1, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kim's Eye Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Selective retina therapy (SRT) selectively disrupts the retinal pigment epithelium (RPE) with minimal damage to the photoreceptors. Previous studies have shown SRT to be effective for resolving SRF, while causing only minimal collateral damage to the retina and vision.However, most patients included in prior studies had chronic CSC (≥3 months symptom duration) and SRT efficacy on acute CSC is not fully known.
The current study evaluated short-term treatment outcomes following SRT with real-time feedback-controlled dosimetry in Korean patients with acute idiopathic CSC.
Detailed Description
Central serous chorioretinopathy (CSC) is a disorder that is characterized by a localized serous detachment of the neurosensory retina in the posterior pole. Additionally, CSC is often self-limiting and spontaneous resolution of subretinal fluid (SRF) often occurs within several months. Although several treatment modalities (e.g., laser photocoagulation, photodynamic therapy, and anti-vascular endothelial growth factor [VEGF] therapy have been used in CSC patients, a consensus has not yet been reached on the optimal time for intervention.
Selective retina therapy (SRT) selectively disrupts the retinal pigment epithelium (RPE) with minimal damage to the photoreceptors. Previous studies have shown SRT to be effective for resolving SRF, while causing only minimal collateral damage to the retina and vision. However, most patients included in prior studies had chronic CSC (≥3 months symptom duration) and SRT efficacy on acute CSC is not fully known.
When treating CSC patients, it is generally recommended to follow-up several months without any intervention to identify spontaneous resolution of SRF. However, prompt treatment may be beneficial for some patients. For example, metamorphopsia or micropsia associated with CSC can greatly interfere with driving or with work when an occupation requires delicate procedures. Additionally, patients are often psychologically distressed by a CSC diagnosis and the accompanying decrease in vision-related quality of life. In these cases, prompt treatment to reduce SRF may relieve, at least in part, CSC symptoms and their related stress.
The current study evaluated short-term treatment outcomes following SRT with real-time feedback-controlled dosimetry in Korean patients with acute idiopathic CSC.
This study included patients who were diagnosed with treatment-naïve idiopathic CSC and were treated with SRT. The R:GEN device (Lutronic, Goyang-si, South Korea) was used to administer SRT. Inclusion criteria also included SRF involving the fovea (documented by optical coherence tomography [OCT] performed at initial presentation) and symptom duration shorter than 3 months. Patients were excluded from analyses if any of the following were true: (1) age > 55 years, (2) clinical or angiographic features suggestive of choroidal neovascularization, (3) OCT findings suggestive of type 1 neovascularization or polypoidal choroidal vasculopathy (e.g., double layer sign or fibrovascular pigment epithelial detachment), (4) history of macular laser photocoagulation, photodynamic therapy, or anti-VEGF therapy, or (5) history of exogenous corticosteroid treatment for a systemic disease (e.g., Cushing's syndrome or renal disease).
Examination, treatment, and follow-up All subjects underwent comprehensive ophthalmologic examinations, including best-corrected visual acuity (BCVA) measurement, slit-lamp biomicroscopy (90-diopter lens), fluorescein angiography (FAG), fundus photography, and spectral domain OCT (Spectralis HRA-OCT™, Heidelberg Engineering, Dossenheim, Germany or RS 3000™, Nidek Co., Ltd., Tokyo, Japan). Indocyanine green angiography using a confocal laser-scanning system (Spectralis HRA-OCT™) was performed at the discretion of each physician. A CSC diagnosis was based on FAG findings, in particular, evidence of a typical ink blot or smokestack leakage. A single examiner (J.H.K.) reviewed all FAG results.
All SRT was performed by a single physician (J.H.K.) using a Nd:YLF laser (wavelength of 257 nm, 15 micro pulses per spot, single micro pulse duration of 1.7 µs, pulse repetition rate of 100 Hz). Spot size was set at a diameter of 200 µm. Real-time feedback-controlled dosimetry (RFD) detects ultrasonic pressure waves generated by intracellular bubble formation and was used to determine optimal laser energy. Before applying laser energy to a leakage point, test shots were made immediately outside of the superior or inferior temporal arcade.
Optimal laser energy was determined based on real-time feedback system indications on the control panel. Laser energy began at 80 µJ and was increased in 5-10 µJ intervals until the optimal energy delivery was confirmed by the RFD system. Following confirmation, the optimal laser energy was applied to fluorescein leakages. If the energy was indeed optimal at leakage points, laser shots were administered around the leakages. If the energy was not optimal at the leakage points, laser energy was again increased in 5-10 µJ increments until optimal energy delivery, as confirmed by the RFD system. If the control panel indicated that excessive laser energy had been applied, the laser energy was decreased in 5-10 µJ increments until the optimal energy delivery was again achieved (confirmed by RFD system). The total number of laser shots delivered around fluorescein leakage points that were at or above the optimal laser energy were counted.
Patients had follow-up visits 1 and 3 months after SRT, at which BCVA was measured and OCT examination was performed. Central foveal thickness (CFT) was manually measured on OCT images and was defined as the distance between the RPE and the internal limiting membrane.
Outcome measures Both BCVA and CFT were measured at diagnosis, at 1 and 3 months following SRT, and at the final follow-up visit. The incidence of complete SRF resolution was estimated. Color fundus photographs taken at each follow-up visit also documented laser treatment and were used to check for the presence of visible laser spots. All BCVA measurements were converted to the logarithm of the minimum angle of resolution (logMAR) for data analyses.
Statistical analyses Statistical analyses were performed using a commercially available software package (SPSS v. 12.0 for Windows; SPSS Inc., Chicago, IL). Comparisons between BCVA and CFT measurements at different time points were performed using Wilcoxon signed-rank tests with a Bonferroni correction. Statistical significance was defined as P ≤ 0.05.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Central Serous Chorioretinopathy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
16 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Treatment arm
Arm Type
Experimental
Arm Description
Patients received selective retina therapy
Intervention Type
Device
Intervention Name(s)
Selective retina therapy
Intervention Description
The selective retina therapy (SRT) is a laser treatment to the retina using the R:GEN device (Lutronic, Goyang-si, South Korea).
Laser energy began at 80 µJ and was increased in 5-10 µJ intervals until the optimal energy delivery was confirmed by the RFD system. Following confirmation, the optimal laser energy was applied to fluorescein leakages. If the energy was indeed optimal at leakage points, laser shots were administered around the leakages. If the energy was not optimal at the leakage points, laser energy was again increased in 5-10 µJ increments until optimal energy delivery.
Primary Outcome Measure Information:
Title
Subretinal fluid
Description
Presence or absence of subretinal fluid which identified based on optical coherence tomography images.
Time Frame
3 months after treatment
Secondary Outcome Measure Information:
Title
Visual acuity
Description
Changes in logarithm of minimal angle of resolution visual acuity during the follow-up, which measured using visual acuity chart.
Time Frame
At diagnosis, at 1 month, and 3 months after treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients diagnosed with treatment-naïve idiopathic central serous chorioretinopathy
Exclusion Criteria:
age > 55 years,
Clinical or angiographic features suggestive of choroidal neovascularization
Optical coherence tomography findings suggestive of type 1 neovascularization or polypoidal choroidal vasculopathy (e.g., double layer sign or fibrovascular pigment epithelial detachment).
History of macular laser photocoagulation, photodynamic therapy, or anti-vascular-endothelial growth factor therapy.
History of exogenous corticosteroid treatment for a systemic disease (e.g., Cushing's syndrome or renal disease).
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
29545953
Citation
Kim YJ, Lee YG, Lee DW, Kim JH. Selective Retina Therapy with Real-Time Feedback-Controlled Dosimetry for Treating Acute Idiopathic Central Serous Chorioretinopathy in Korean Patients. J Ophthalmol. 2018 Feb 6;2018:6027871. doi: 10.1155/2018/6027871. eCollection 2018.
Results Reference
derived
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Selective Retina Therapy With Real-Time Feedback-Controlled Dosimetry for Treating Acute Idiopathic Central Serous Chorioretinopathy in Korean Patients
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