Skip to content

Clinical observation of 577nm micropulse laser combined with traditional Chinese medicine in the treatment of acute Central serous chorioretinopathy

Clinical observation of 577nm micropulse laser combined with traditional Chinese medicine in the treatment of acute Central serous chorioretinopathy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070688
Enrollment
Unknown
Registered
2023-04-20
Start date
2021-10-01
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

Central serous chorioretinopathy

Interventions

577nm micropulse combined with TCM treatment group (within 500um):577nm micropulse combined with TCM treatment
577nm micropulse trearment group (within 500um):577nm micropulse trearment
Traditional Chinese medicine treatment group (within 500um):Traditional Chinese medicine treatment
blank control group (within 500um):N/A
Normal laser treatment group (beyond 500um):Conventional 532nm laser therapy
577nm micropulse trearment group (beyond 500um):577nm micropulse combined with TCM treatment
blank control group (beyond 500um):N/A

Sponsors

Lanzhou Aier Eye Housipital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
37 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Young and middle-aged patients; (2) aCSC was diagnosed by routine ophthalmic examination, fluorescent retinal angiography and OCT; (3) Onset time <6 months

Exclusion criteria

Exclusion criteria: (1) Unstable systemic diseases, including uncontrollable infections, body temperature >=38 degree, etc.; (2) Liver and kidney dysfunction; (3) pregnant and lactating women; (4) Investigators with poor compliance or severe mental or language disorders who are unable to complete the clinical trial protocol; (5) Those who have participated in clinical trials of other drugs in the past 3 months; (6) Patients with severe eye diseases such as glaucoma and uveitis (7) disagreed with the treatment plan; (8) Cases with incomplete data

Design outcomes

Primary

MeasureTime frame
macular central foveal thickness;best corrected visual acuity;

Secondary

MeasureTime frame
choroid central thickness;choroid paracentral thickness;

Countries

china

Contacts

Public ContactWenjuan Duan

Lanzhou Aier Eye Housipital

13919441095@163.com+8613919441095

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026