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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: IRCT
Last refreshed on: 22 February 2018
Main ID:  IRCT201201278832N1
Date of registration: 2012-12-19
Prospective Registration: No
Primary sponsor: Gonabad University of Medical Sciences
Public title: Evaluation of saffron effect on intraocular pressure in glaucoma patients
Scientific title: The Ocular Hypotensive Effect of Saffron Extract in Primary Open Angle Glaucoma: a Pilot Study
Date of first enrolment: 2012-02-22
Target sample size: 15
Recruitment status: Complete
URL:  http://en.irct.ir/trial/9320
Study type:  interventional
Study design:  Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment.  
Phase:  2
Countries of recruitment
Iran (Islamic Republic of)
Contacts
Name: Mohammad Hossein Jabbarpoor Bonyadi   
Address:  22 Bahman Hospital Gonabad Iran (Islamic Republic of)
Telephone: +98 53 3722 9012
Email: drbonyadi@gmu.ac.ir
Affiliation:  Gonabad University of Medical Sciences
Name: Mohammad Hossein Jabbarpoor Bonyadi   
Address:  Gadir square Gonabad Gonabad Iran (Islamic Republic of)
Telephone: +98 53 3722 9012
Email: drbonyadi@gmu.ac.ir
Affiliation:  Gonabad University of Medical Sciences
Key inclusion & exclusion criteria
Inclusion criteria: inclusion criteria :open angle glaucoma; age >50
exclusioncriteria: angle closure glaucoma; systemic componding medication

Exclusion criteria:

Age minimum: 50 years
Age maximum: no limit
Gender: Both
Health Condition(s) or Problem(s) studied
primary open angle glaucoma.
Primary open-angle glaucoma
Primary open-angle glaucoma
Intervention(s)
saffron capsule daily( 30 mg)
placebo capsule daily
Intervention 1: placebo capsule daily. Intervention 2: saffron capsule daily( 30 mg).
Treatment - Drugs
Primary Outcome(s)
Intraocular pressure. Timepoint: baseline,7th,21th and 28th day after 1 month wash-out. Method of measurement: goldmann tonometery.
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
Gonabad University of Medical Sciences
Secondary Sponsor(s)
Ethics review
Status: Approved
Approval date:
Contact:
Ethics committee of Gonabad University of Medical Sciences
Results
Results available:
Date Posted:
Date Completed:
URL:
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