NCT02146599
Completed
Not Applicable
Patient Perception of Visual Quality and Function
ConditionsCataract
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Cataract
- Sponsor
- Abbott Medical Optics
- Enrollment
- 301
- Locations
- 1
- Primary Endpoint
- Use of Corrective Visual Aids (i.e., Spectacles, Contact Lenses) Post Intraocular Lens (IOL) Surgery
- Status
- Completed
- Last Updated
- 10 years ago
Overview
Brief Summary
The purpose of this study is to evaluate the visual quality and function of pseudophakic patients.
Investigators
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
Outcomes
Primary Outcomes
Use of Corrective Visual Aids (i.e., Spectacles, Contact Lenses) Post Intraocular Lens (IOL) Surgery
Time Frame: Baseline and 1 week
Patients will be assessed at a baseline visit and a visit 1 week later to determine their use of corrective visual aids (i.e., spectacles, contact lenses) post Intraocular Lens (IOL) surgery.
Study Sites (1)
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