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Effect of crocin on ocular complications of Behcet's disease

Pilot Study on the effectiveness of crocin as a drug supplement in the treatment of ocular complications of Behcet's disease; a clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130418013058N12
Enrollment
40
Registered
2019-05-18
Start date
2019-02-19
Completion date
Unknown
Last updated
2019-08-26

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

Conditions

Behcet's Disease. Behcet's disease

Interventions

Intervention 1: Intervention group: Receiving one tablet of Crocin (15 mg) for three months. Intervention 2: Control group: Receiving one tablet of placebo for three months.

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: A patient with active Behcet's with ocular complications is selected according to the sun criteria, Patients with Behcet's syndrome with anterior, posterior, or diffuse eye involvement Long-term illness of the eye with active retinal vasculitis and macular edema Age over 18 years of both sexes A patient with Behcet's who is resistant (without improvement or exacerbation of the eye disease) or an approximate response (mild to moderate) to combination therapy (Psychosis and Steroids drugs) The ability to understand the overall study, interventions and possible complications

Exclusion criteria

Exclusion criteria: Patients with bilateral vision loss Patients receiving anti-TNF drugs such as thalidomide and pentoxifylline in the past three months. Patients with a history of immunosuppression include a viral infection such as tuberculosis Severe viral infections including hepatitis, pneumonia, pyelonephritis, or hepatitis in the last three months Pregnancy and breastfeeding Sensitivity to saffron alcohol consumption Cataract and other general items Diabetes

Design outcomes

Primary

MeasureTime frame
Ocular Inflammation. Timepoint: Before Intervention, and after three months. Method of measurement: Fluorescein Angiography.

Secondary

MeasureTime frame
Best Corrected Visual Acuity. Timepoint: Before Intervention, and After Three Months. Method of measurement: Snellen Chart.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Seyed Ahmad Mohajeri

Mashhad University of Medical Sciences

mohajeria@mums.ac.ir+98 51 3882 3251

Outcome results

None listed

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