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Clinical Trials/CTRI/2024/06/069496
CTRI/2024/06/069496Not yet recruitingUnknown

Correlation of central and peripheral contrast sensitivity with higher order aberrations in computer vision syndrome - NI

Government Medical College and Hospital0 sites0 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
Unknown
Status
Not yet recruiting
Sponsor

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Observational

Eligibility Criteria

Inclusion Criteria

  • SUBJECT SELECTION
  • Group 1: Normal Controls
  • Group 2: Patients with Computer Vision Syndrome
  • INCLUSION CRITERIA FOR GROUP 1
  • 1. Age more than 18 and less than 40 years, either gender
  • 2. Best corrected visual acuity of 6/6 and near acuity of N6.
  • 3. No signs or symptoms of CVS
  • INCLUSION CRITERIA FOR GROUP 2
  • 1. Age more than 18 and less than 40 years, either gender
  • 2. Best corrected visual acuity of 6/6 and near acuity of N6.
  • 3. Having a score of more than 6 in the CVS-Q questionnaire

Exclusion Criteria

  • 1. Contact lens use
  • 2. Patients with history of incisional or laser eye surgery
  • 3. Any cause for visual impairment (e.g., glaucoma, cataract more than grade 2 or higher
  • using LOCS III grading (Annexure 3), diabetic retinopathy, Age Related Macular
  • Degeneration, etc.) or media opacities.
  • 4. Patients with amblyopia; strabismus; anisometropia; refractive errors higher than 6 D
  • myopia, 4 D hyperopia, or 4 D astigmatism
  • 5. Any medical condition which in the investigators opinion would preclude the patient
  • from providing reliable and valid data (e.g., cognitive impairment, Parkinsons disease,
  • Alzheimers disease and any other neurological or musculoskeletal disease).

Investigators

Sponsor
Government Medical College and Hospital

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