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Clinical Trials/IRCT20110811007297N7
IRCT20110811007297N7
Recruiting
Phase 2

Efficacy and Safety of Crocin Supplementation in Patients With Central SerousChorioretinopathy (CSCR)

Shiraz University of Medical Sciences0 sites40 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Central serous chorioretinopathy.
Sponsor
Shiraz University of Medical Sciences
Enrollment
40
Status
Recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • age of 18\-60 years old
  • The diagnosis of CSCR based on clinical and imagining evaluation
  • informed consent

Exclusion Criteria

  • Chronic Central SerousChorioretinopathy (CSCR)
  • Laser treatment (6 months prior to enrollment)
  • Intravitreal injection (3 months prior to enrollment)
  • Other retinal diseases
  • History of eye diseases
  • Diabetes Mellitus
  • Renal or hepatic diseases
  • Allergy to saffron or crocin
  • Pregnancy or lactation
  • Beta\-blocker, diuretic, or corticosteroid (1 week prior to enrollment)

Outcomes

Primary Outcomes

Not specified

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