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The Safe Effective Light Dose of Photodynamic Therapy for Chronic Central Serous Chorioretinopathy

The Safe Effective Light Dose of Photodynamic Therapy for Chronic Central Serous Chorioretinopathy

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01630863
Enrollment
45
Registered
2012-06-28
Start date
2012-06-30
Completion date
2015-03-31
Last updated
2015-02-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Central Serous Chorioretinopathy

Keywords

Central serous chorioretinopathy, photodynamic therapy, safe and effective dose

Brief summary

To find the safe effective lowest light dose for photodynamic therapy (PDT). in the treatment of central serous chorioretinopathy.

Interventions

PROCEDUREPhotodynamic therapy

Photodynamic therapy is performed using verteporfin. Full dose of verteporfin is infused for 10 minutes, followed by laser delivery at 15 minutes from the start of infusion. Different light dose of PDT is applied to the patients at 50%, 40% and 30% of the full energy based on TAP study. The area of irradiation is set to the abnormal choroidal vascular hyperpermeability on ICGA corresponding to the leaking area on FA.

Sponsors

Yeungnam University College of Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

1. Idiopathic detachment of the neurosensory retina with a focal leak at the level of the RPE with FA 2. Presence of SRF and/or serous pigment epithelial detachment on optical coherence tomography (OCT) 3. Presence of abnormal dilated choroidal vasculature in ICGA 4. Patients with symptomatic CSC of at least 3 months duration

Exclusion criteria

1. Patients who received any previous treatment, including PDT or focal thermal laser photocoagulation for CSC, or who had evidence of CNV, PCV, or other maculopathy on clinical examination, FA, or ICGA 2. Patients receiving exogenous corticosteroid treatment 3. Patients with systemic diseases such as Cushing's disease or renal diseases 4. Pregnant patients

Design outcomes

Primary

MeasureTime frameDescription
Changes of best corrected visual acuity6 monthChanges of best corrected visual acuity at baseline and 1, 3, 6 month after PDT

Secondary

MeasureTime frameDescription
Change of central retinal thickness, success rate, recurrence rate, and complications6 monthsChange of the central retinal thickness on optical coherence tomography (OCT)are compared at baseline at 1, 3, and 6 months after PDT. Additionally, success rate, recurrence rate, and complications between three groups are evaluated during 6 months.

Countries

South Korea

Contacts

Primary ContactMin Sagong
msagong@ynu.ac.kr82-53-620-4191

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026