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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: |
IRCT2015040418966N3 |
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Date of registration:
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2015-04-09 |
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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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The removal of the foreign bodies from the eye by surgical methods
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Scientific title:
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Removal of Intraocular Foreign Bodies by Pars Plana Vitrectomy - Outcomes and Prognostic Factors |
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Date of first enrolment:
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2009-01-01 |
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Target sample size:
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30 |
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Recruitment status: |
Complete |
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URL:
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http://en.irct.ir/trial/17074 |
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Study type:
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interventional |
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Study design:
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Randomization: N/A, Blinding: Not blinded, Placebo: Not used, Assignment: Single, Purpose: Treatment, Other design features: The associated lesions produced by the intraocular foreign bodies are analyzed.
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Phase:
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0 (exploratory trials)
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Countries of recruitment
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Romania
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Contacts
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Name:
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Simona Delia Nicoara
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Address:
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8, V. Babes str.
Cluj-Napoca
Romania |
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Telephone:
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0040264596585 |
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Email:
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simoananicoara1@gmail.com |
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Affiliation:
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Iuliu Hatieganu University of Medicine and Pharmacy |
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Name:
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Simona Delia Nicoara
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Address:
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8, V. Babes str.
Cluj-Napoca
Romania |
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Telephone:
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0040264547681 |
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Email:
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stalu@umfcluj.ro |
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Affiliation:
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Iuliu Hatieganu University of Medicine and Pharmacy |
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Key inclusion & exclusion criteria
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Inclusion criteria: Inclusion criteria: all the patients in which pars plana vitrectomy was performed in order to extract intraocular foreign bodies.
Exclusion criteria: patients that failed the control visit.
Exclusion criteria:
Age minimum:
18 years
Age maximum:
85 years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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H.44.6
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Intraocular Foreign Bodies.
H.44.6
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Intervention(s)
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Treatment - Surgery
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We had no control group
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We had no control group.
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Primary Outcome(s)
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Visual acuity (vision). Timepoint: 6 months after treatment. Method of measurement: Visual acuity test with Snellen chart.
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Secondary Outcome(s)
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Appearance of the eye. Timepoint: 6 months after treatment. Method of measurement: Biomicroscopy of the anterior and posterior segments of the eye.
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Source(s) of Monetary Support
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Investigator
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Ethics review
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Status: Approved
Approval date:
Contact:
Ethics Commitee of the "Iuliu Hatieganu" University of Medicine and Pharmacy
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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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