Efficacy and Safety of Crocin Supplementation in Patients With Central Serous Chorioretinopathy (CSCR)
Who is this study for? Patients with central serous chorioretinopathy
What treatments are being studied? Crocin
Status: Unknown
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1
SUMMARY
Preclinical and clinical evidence support the protective effect of crocin on different pathologic pathways involved in central serous chorioretinopathy (CSCR). They involve inflammation, oxidative stress, mineralocorticoid pathway, and also stress-related injuries. It also showed that crocin has a protective effect on the retinal pigmented epithelium (RPE) layer. Based on the mentioned evidence the study designed to evaluate the efficacy and safety of 2-month crocin supplementation (15 mg/d) in 40 patients with CSCR in a randomized controlled blinded clinical trial.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 60
Healthy Volunteers: f
View:
• age of 18-60 years old
• The diagnosis of CSCR based on clinical and imagining evaluation
• informed consent
Locations
Other Locations
Islamic Republic of Iran
Shiraz University of Medical Sciences
RECRUITING
Shiraz
Time Frame
Start Date: 2021-07-01
Completion Date: 2021-11-30
Participants
Target number of participants: 40
Treatments
Experimental: Crocin
Placebo_comparator: Placebo
Related Therapeutic Areas
Sponsors
Leads: Shiraz University of Medical Sciences