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Comparison of Multiple Treatments on Central Serous Chorioretinopathy and Their Prognostic Factors

Comparison of Multiple Treatments on Central Serous Chorioretinopathy and Their Prognostic Factors

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100044356
Enrollment
Unknown
Registered
2021-03-17
Start date
2021-03-30
Completion date
Unknown
Last updated
2021-09-07

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

Conditions

Central Serous Chrioretinopathy

Interventions

1:Subthreshold micropulse laser
2:Spironolactone

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. aged >= 18 years; 2. Diagnosed with chronic CSC (>3 months); 3. The presence of subretinal fluid (SRF) on OCT; 4. Accept monthly follow-up for at least 9 months.

Exclusion criteria

Exclusion criteria: 1. Patients with other ocular diseases, especially fundus diseases; 2. Myopia above -6D; 3. Had intraocular surgery in the past 3 months, using or have used corticosteroids in the past 6 months, have received anti-VEGF therapy in the past 6 months, have received traditional laser treatment in the past 1 year, or planning to use corticosteroids within six months after receiving treatment; 4. Those who cannot accept monthly follow-up; 5. Patients with FA and ICGA contraindications, such as pregnancy, liver and kidney dysfunction, allergy to contrast agents, etc.; 6. Serum potassium >= 5.5mmol/L; 7. Taking angiotensinase inhibitors; 8. Female patients who plan to become pregnant within 9 months after treatment.

Design outcomes

Primary

MeasureTime frame
Percentage of Complete Resolution of SRF;

Secondary

MeasureTime frame
Change of BCVA;Change of CMT;Change of SFCT;Change of SRF Height;Second treatment;

Countries

China

Contacts

Public ContactMeixia Zhang

West China Hospital of Sichuan University

zhangmeixia@scu.edu.cn+86 18980602236

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 5, 2026