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Angiographic Characteristics of CSC, PCV Patients and Thrombotic Bio-markers

Analysis of Plasminogen Activator Inhibitor-1 Level in Chronic Serous Chorioretinopathy and Polypoidal Choroidal Vasculopathy

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02815176
Enrollment
100
Registered
2016-06-28
Start date
2016-06-30
Completion date
2017-06-30
Last updated
2016-06-29

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

Conditions

Central Serous Chorioretinopathy, Polypoidal Choroidal Vasculopathy

Keywords

Plasminogen activator inhibitor-1, Wide angle fluorescein angiography, Choroid

Brief summary

Thrombotic biomarkers and angiographic characteristics were compared among the de novo patients of central serous chorioretinopathy (CSC), polypoidal choroidal vasculopathy (PCV) and the control.

Interventions

OTHERBlood sampling

Sampling the blood including DNA to investigate the thrombotic profile

Sponsors

Samsung Medical Center
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* CSC * neurosensory detachment in optical coherence tomography (OCT) * focal leakage in fluorescein angiography (FAG) and/or late choroidal hyperpermeability in indocyanine green angiography (ICGA) * PCV * subretinal and/or sub-retinal pigment epithelial fluid in OCT * branching vascular network and/or polyps in ICGA * Control * epiretinal membrane (ERM) * without underlying systemic, ophthalmic disease other than ERM

Exclusion criteria

* Previous history of using steroid (oral, topical) * Previous history of CSC/PCV * Previous history or evidence of intraocular inflammation including uveitis * Co-existing retinal or choroidal diseases * History of allergic reaction to fluorescein or indocyanine green dye * Underlying systemic conditions that could affect the thrombotic profiles (e.g. diabetes, hypertension, metabolic syndrome, coronary artery disease, cerebrovascular diseases, stroke, chronic renal failure, current smoker, pregnancy, sleep disorder)

Design outcomes

Primary

MeasureTime frameDescription
Serum PAI-1 SNP genotyping in active PCV and CSC patientsLess than 1 week after initial diagnosisSerum PAI-1 SNP(single nucleotide polymorphism) genotyping
Serum Fibrin degradation product in active PCV and CSC patientsLess than 1 week after initial diagnosisSerum Fibrin degradation product (μg/mL)
Serum PAI-1 antigen in active PCV and CSC patientsLess than 1 week after initial diagnosisSerum PAI-1 (plasminogen activator inhibitor-1) antigen (ng/mL)
Serum Fibrinogen in active PCV and CSC patientsLess than 1 week after initial diagnosisSerum Fibrinogen (mg/dl)
Serum Factor VIII activity in active PCV and CSC patientsLess than 1 week after initial diagnosisSerum Factor VIII activity (%)
Serum Plasminogen activity in active PCV and CSC patientsLess than 1 week after initial diagnosisSerum Plasminogen activity (%)
Serum D-dimer in active PCV and CSC patientsLess than 1 week after initial diagnosisSerum D-dimer (μg/mL(FEU))

Secondary

MeasureTime frameDescription
Characteristics of indocyanine green angiography in active PCV and CSC patientsLess than 1 week after initial diagnosisNumbers of hyperfluorescent spots in indocyanine green angiography
Characteristics of fluorescein angiography in active PCV and CSC patientsLess than 1 week after initial diagnosisNumbers of leaking points of fluorescein dye in fluorescein angiography

Countries

South Korea

Contacts

Primary ContactSe Woong Kang, MD
swkang@skku.edu+82-2-3410-3548

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026