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Comparison Between Myopia Versus Hypermetropia With Progressive Addition Lenses in Computer Users

S

Superior University

Status

Active, not recruiting

Conditions

Myopia
Hypermetropia

Treatments

Other: Hypermetropia
Behavioral: Myopia

Study type

Interventional

Funder types

Other

Identifiers

NCT06484257
MSRSW/Batch-Fall22/732

Details and patient eligibility

About

This study examines how myopia (nearsightedness) and hyperopia (farsightedness) affect the use of progressive addition lenses (PALs) for computer users. PALs offer a range of vision correction within one lens, ideal for presbyopia (age-related near focusing difficulty). We'll compare visual comfort, eye strain, and user preference for PALs between myopic and hyperopic individuals while focusing on computer screens.

Full description

The research will also consider if general-purpose PALs differ from computer-specific PALs in these user groups, and how presbyopia progression might influence PAL effectiveness for each condition. This information can help eye doctors recommend the most suitable PAL design for computer users with myopia or hyperopia.

Enrollment

64 patients

Sex

All

Ages

40 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The age of Participant will be 40 to 55 years
  • Participant diagnosed with myopia having -0.50 to -3.00DS and astigmatism up to -0.75DC
  • Patient diagnosed with Hypermetropia having +050 to +3.00 DS and Astigmatism up to +0.75DC
  • Presbyopia addition will range from +1.00 to +2.50 DS
  • Participants who have worked more than 4 hours on the computer screen.
  • Participants who will be already progressive users and first-time users.
  • Patients with no Ocular disease.

Exclusion criteria

  • Participants with Pre Presbyopia and above 55 years of age
  • Participants with significant ocular disease.
  • Participants with uncontrolled diabetes and hypertension
  • Participants who will not be willing for PAL,s
  • Participants with more than 0.75 astigmatism
  • Participants with known allergies and sensitivity.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

64 participants in 2 patient groups

Myopia
Active Comparator group
Treatment:
Behavioral: Myopia
Hypermetropia
Other group
Treatment:
Other: Hypermetropia

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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