Health Condition 1: H527- Unspecified disorder of refraction
Conditions
Interventions
Control Intervention1: NIL: NIL
Sponsors
Sankara Academy of Vision
Eligibility
Inclusion criteria
Inclusion criteria: Participants who can understand and provide informed consent for participation in the study. Participants above 8 years old. All Genders are included. Participant is willing and able to follow all study procedures and requirements.
Exclusion criteria
Exclusion criteria: Patients with spherical power above +/-18.00D and cylindrical power above +/-6.00D Pregnant women is excluded Patient who is under medication known to significantly affect the vision Patient who is undergone eye surgery within 3 months before the participation in the study including LASIK or Lens replacement Patient who has eye pathologies like conjunctivitis, keratitis. herpes and eye injury
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Difference between spherical, cylindrical measurements & axis alignment obtained by the 3nethra Specto and those obtained by subjective refraction using trial frame and Difference between spherical, cylindrical measurements & axis alignment obtained by the 3nethra Specto and those obtained by the Topcon Phoropter.Timepoint: In one visit at a time span of 1 hour | — |
Secondary
| Measure | Time frame |
|---|---|
| Repeatability (Precision) of Measurements: The consistency of spherical, cylindrical, and axis measurements obtained by the 3nethra Specto over two repeated tests. Time Efficiency: The time taken to complete the refraction process with the 3nethra Specto compared to the time taken using subjective refraction with a trial frame. Patient Comfort: Patient-reported comfort levels during the refraction process with the 3Nethra Specto, assessed using a standardized comfort questionnaire.Timepoint: In one visit at a time span of 1 hour | — |
Countries
India
Contacts
Public ContactKaushik Murali
Sankara Eye Hospital
Outcome results
None listed