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Main
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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. |
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Register:
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IRCT |
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Last refreshed on:
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22 February 2018 |
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Main ID: |
IRCT201401148410N2 |
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Date of registration:
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2014-09-10 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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trabeculectomy with releasable sutures in treatment of glaucoma
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Scientific title:
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comparison of trabeculectomy with releasable sutures and standard trabeculectomy in treatment of glaucoma |
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Date of first enrolment:
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2011-12-31 |
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Target sample size:
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28 |
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Recruitment status: |
Complete |
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URL:
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http://en.irct.ir/trial/8881 |
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Study type:
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interventional |
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Study design:
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Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment.
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Phase:
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N/A
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Countries of recruitment
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Iran (Islamic Republic of)
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Contacts
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Name:
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Dr Ahmad Sarvarian
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Address:
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Amir Kabir Hospital, Parastar Square
Arak
Iran (Islamic Republic of) |
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Telephone:
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+98 86 3313 5075 |
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Email:
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dr.ahsarvarian@arakmu.ac.ir |
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Affiliation:
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Arak University of Medical Sciences |
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Name:
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Dr Ahmad Sarvarian
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Address:
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Amir Kabir Hospital, Parastar Square
Arak
Iran (Islamic Republic of) |
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Telephone:
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+98 86 3313 5075 |
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Email:
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dr.ahsarvarian@arakmu.ac.ir |
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Affiliation:
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Arak University of Medical Sciences |
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Key inclusion & exclusion criteria
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Inclusion criteria: inclusion criteria:Primary open angle glaucoma; primary angle closure glaucoma who didn't Respond to medication
exclusion criteria: uveitic; post-traumatic; neovascular; Juvenile glaucoma; Previous ophthalmic surgery; combined procedures (glaucoma and cataract)
Exclusion criteria:
Age minimum:
no limit
Age maximum:
no limit
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Glaucoma.
Primary open-angle glaucoma
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Primary open-angle glaucoma
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Intervention(s)
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patients of second group undergo standard trabeculectomy. 24 hour after surgery anterior chamber depth, intraocular pressure, hyphema and iridocorneal touch will evaluate.
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Intervention 1: patients of first group undergo trabeculectomy with releasable sutures. 24 hour after surgery anterior chamber depth, intraocular pressure, hyphema and iridocorneal touch will evaluate. Intervention 2: patients of second group undergo standard trabeculectomy. 24 hour after surgery anterior chamber depth, intraocular pressure, hyphema and iridocorneal touch will evaluate.
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Treatment - Surgery
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patients of first group undergo trabeculectomy with releasable sutures. 24 hour after surgery anterior chamber depth, intraocular pressure, hyphema and iridocorneal touch will evaluate.
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Primary Outcome(s)
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Intraocular pressure. Timepoint: before trabeculectomy and 24 hours after trabeculectomy. Method of measurement: Goldmann tonometry.
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Secondary Outcome(s)
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Corneal edema. Timepoint: 24 hours after trabeculectomy. Method of measurement: observation with slit lamp.
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Shallow anterior chamber. Timepoint: 24 hours after trabeculectomy. Method of measurement: measurement with slit lamp.
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Hyphema. Timepoint: 24 hours after trabeculectomy. Method of measurement: observation with slit lamp.
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Iridocorneal touch. Timepoint: 24 hours after trabeculectomy. Method of measurement: observation with slit lamp.
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Source(s) of Monetary Support
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Arak University of Medical Sciences, Vice chancellor for research
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Ethics review
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Status: Approved
Approval date:
Contact:
Ethics Committee of the arak university of medical sciences
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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