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Computer Vision Syndrome Visual Sequelae

NCT04398212 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 733

Last updated 2020-08-10

No results posted yet for this study

Summary

the university students will respond to CVS-F3 survey form and then they will be subjected to complete ophthalmic examination and investigations

Conditions

  • Computer Vision Syndrome

Interventions

DIAGNOSTIC_TEST

mfERG (multifocal-retinogram)

mfERG will be performed for the students to document the effect of CVS on retina

Sponsors & Collaborators

  • Sohag University

    lead OTHER

Principal Investigators

  • Mohammed Iqbal, MD. PhP · Sohag University

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
SINGLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-05-21
Primary Completion
2020-06-15
Completion
2020-08-01

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04398212 on ClinicalTrials.gov