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N/A N=301

Patient Perception of Visual Quality and Function

Cataract

Enrolled (actual)
301
Serious AEs
0.0%
Results posted
Sep 2015
Primary outcome: Primary: Use of Corrective Visual Aids (i.e., Spectacles, Contact Lenses) Post Intraocular Lens (IOL) Surgery — 71; 8; 9 participants

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Administration of patient self-assessment (Other)
Age
Adult, Older Adult · 22+ yrs
Sex
All
Sponsor
Abbott Medical Optics
Primary completion
Jul 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Use of Corrective Visual Aids (i.e., Spectacles, Contact Lenses) Post Intraocular Lens (IOL) Surgery
71; 8; 9

Summary

The purpose of this study is to evaluate the visual quality and function of pseudophakic patients.

Eligibility Criteria

Inclusion Criteria

  • Minimum 22 years of age
  • Pseudophakic patients who have been bilaterally implanted with the same type of intraocular lenses in both eyes
  • Ability to understand, read and write English to give consent and complete the study questionnaires
  • Availability, willingness, and sufficient cognitive awareness to comply with examination procedures and study visits
  • Signed informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization
  • Other protocol-defined inclusion criteria might apply

Exclusion Criteria

  • Any ocular pathology of clinical significance, as determined by the investigator, that may affect visual outcomes or influence subjective ocular/visual symptoms
  • Patient is pregnant or is lactating
  • Concurrent participation or participation within 30 days prior in any other clinical trial
  • Other protocol-defined exclusion criteria might apply
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02146599). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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