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Clinical treatment and analysis of risk factors of central serous chorioretinopathy

Clinical treatment and analysis of risk factors of central serous chorioretinopathy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-16008428
Enrollment
Unknown
Registered
2016-05-06
Start date
2013-07-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

central serous chorioretinopathy

Interventions

I(acute CSC):observation
II(acute CSC):oral spironolactone
III(chronic CSC):oral spironolactone

Sponsors

The First Affiliated Hospital of Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.FFA showing a focal leak at the level of the RPE,a subretinal detachment of the retinal photoreceptors from the RPE layer was demonstrated by spectral-domain OCT; 2.patients aged >=18 years; 3.existence of subretinal fluid (SRF) with subjective symptoms such as decreased vision or metamorphopsia.

Exclusion criteria

Exclusion criteria: 1. current pregnancy; 2. history of taking corticosteroids or related drugs; 3. systemic diseases such as endogenous hypercortisolism, and diabetic; 4. Macular disorders such as idiopathic choroidal neovascularization, polypoidal choroidal vasculopathy, and age-related macular degeneration were excluded from the study; 5. eyes with a history of previous treatment, including macular photocoagulation, photodynamic therapy, or intravitrealantivascular endothelial growth factor injection, also were excluded; 6. High blood pressure, diabetes, hyperlipidemia and other systemic diseases.

Design outcomes

Primary

MeasureTime frame
BCVA;OCT;aldosterone level;

Countries

China

Contacts

Public ContactQinghuai Liu

The First Affiliated Hospital of Nanjing Medical University

liuqh@njmu.edu.cn+86 13901585755

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 25, 2026