Prospective Geometric Analysis of Ultra-Widefield OCTA Characteristics in Central Serous Chorioretinopathy Patients

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-60
SponsorSun Yat-sen University

About this trial

By leveraging parameters including fractal dimension and topological index, we constructed a quantitative evaluation framework for ultra-widefield optical coherence tomography angiography (UWF-OCTA) images in patients with central serous chorioretinopathy (CSC), thus overcoming the limitations of conventional qualitative analysis.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Adults aged 18 to 60 years, inclusive;

Clinical diagnosis of central serous chorioretinopathy (CSC);

Completion of fundus fluorescein angiography (FFA) and indocyanine green angiography (ICGA) examinations;

Completion of ultra-widefield optical coherence tomography angiography (UWF-OCTA) imaging;

Disqualifiers

Presence of systemic diseases that may affect study outcomes or participant safety;

Pregnant or lactating women;

History of psychiatric or mental disorders that may impair compliance;

Hemorrhagic diathesis or requirement for long-term anticoagulant therapy;

Trial population

The study subjects were recruited from outpatients of the Medical Retina Department at Zhongshan Ophthalmic Center, and eligible cases meeting the study criteria were selected from the outpatient medical record system.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

120 Participants
are grouped into 4 trial groups
Group A: Acute Central Serous Chorioretinopathy
Group B: Chronic Central Serous Chorioretinopathy
Group C: Recurrent Central Serous Chorioretinopathy
Group D: Control Group

Trial outcomes

Primary outcomes

1

Choroidal Vascular Fractal Dimension

Choroidal vascular fractal dimension quantified from optical coherence tomography angiography (OCTA) images.

Time frame
Baseline, 1 month, 3 months, 6 months, and 12 months

Secondary outcomes

1

Maximum subretinal fluid height

The maximum height of subretinal fluid measured in micrometers (μm) on optical coherence tomography angiography (OCTA) images.

Time frame
Baseline, 1 month, 3 months, 6 months, and 12 months
2

Subretinal fluid area

The basal area of subretinal fluid measured in square millimeters (mm²) on optical coherence tomography angiography (OCTA) images.

Time frame
Baseline, 1 month, 3 months, 6 months, and 12 months
3

Subretinal fluid volume

The volume of subretinal fluid measured in cubic millimeters (mm³) on optical coherence tomography angiography (OCTA) images.

Time frame
Baseline, 1 month, 3 months, 6 months, and 12 months
4

Choroidal vascular branching index

The branching index of choroidal blood vessels quantified from optical coherence tomography angiography (OCTA) images.

Time frame
Baseline, 1 month, 3 months, 6 months, and 12 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: