Central Serous Chorioretinopathy Clinical Trials

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the Study of the Association Between the Gut Microbiota and Central Serous Chorioretinopathy

Status: Recruiting
Location: See location...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

To investigate the potential association between gut microbiota and central serous chorioretinopathy (CSC), clinical observations have indicated that patients with CSC frequently present with chronic gastrointestinal symptoms. This observation has led to the hypothesis that CSC may be associated with gut dysbiosis. The genus Bifidobacterium is widely recognized as a beneficial component of the gut microbiota, and multiple well-established Bifidobacterium supplements are commercially available. To explore this potential association, fecal samples will be collected from both CSC patients and healthy controls. Whole-metagenome shotgun sequencing will be performed to compare gut microbial compositions between the two groups and to determine whether significant differences exist. In addition, CSC patients will be randomly assigned to two groups. One group will receive Bifidobacterium supplementation for a minimum of one month, while the other group will receive a placebo. Clinical outcomes will then be evaluated to assess whether Bifidobacterium supplementation is associated with faster recovery and reduced relapse rates compared with placebo.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: t
View:

• Age 18 to 60 years

• Diagnosis of acute central serous chorioretinopathy (CSC) (affected eye: ① FFA and ICGA showing typical CSC manifestations, ② presence of subretinal fluid (SRF) at the macular fovea, ③ disease duration ≤ 6 months)

• Best Corrected Visual Acuity (BCVA): 53 to 86 letters

• Other: No significant systemic diseases, signed informed consent, and able to commit to follow-up

Locations
Other Locations
China
2 nd Affiliated Hospital, School of Medicine, Zhejiang University, China
RECRUITING
Hanzhou
Contact Information
Primary
Weixin Zheng, master
22318933@zju.edu.cn
+86 18888918935
Backup
Panpan Ye, doctor
yepanpan@zju.edu.cn
+86 13806506267
Time Frame
Start Date: 2026-05-27
Estimated Completion Date: 2028-07-01
Participants
Target number of participants: 400
Treatments
Experimental: receiving Bifidobacterium supplements
Placebo_comparator: receiving placebo
Related Therapeutic Areas
Sponsors
Leads: Second Affiliated Hospital, School of Medicine, Zhejiang University

This content was sourced from clinicaltrials.gov