Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
733 participants
INTERVENTIONAL
2018-05-21
2020-08-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
DIAGNOSTIC
SINGLE
Study Groups
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Non-complaining group
the students in this group are not complaining of CVS symptoms but will be examined to diagnose CVS or exclude it
mfERG (multifocal-retinogram)
mfERG will be performed for the students to document the effect of CVS on retina
Complaining group
the students in this group are complaining of CVS symptoms but will be examined to document their complains and correlate to clinical findings
mfERG (multifocal-retinogram)
mfERG will be performed for the students to document the effect of CVS on retina
Interventions
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mfERG (multifocal-retinogram)
mfERG will be performed for the students to document the effect of CVS on retina
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Anisometropia
* strabismus
* Previous eye surgery
ALL
No
Sponsors
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Sohag University
OTHER
Responsible Party
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Prof. Mohammed Iqbal
Assistant Professor of Ophthalmology
Principal Investigators
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Mohammed Iqbal, MD. PhP
Role: PRINCIPAL_INVESTIGATOR
Sohag University
Locations
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Faculty of medicine
Sohag, , Egypt
Countries
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Other Identifiers
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5-10/4/2018
Identifier Type: -
Identifier Source: org_study_id
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