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Patient Perception of Visual Quality and Function

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Abbott

Status

Completed

Conditions

Cataract

Treatments

Other: Administration of patient self-assessment

Study type

Observational

Funder types

Industry

Identifiers

NCT02146599
QPRO-101-SIVQ

Details and patient eligibility

About

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

Enrollment

301 patients

Sex

All

Ages

22+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

301 participants in 1 patient group

Pseudophakic
Treatment:
Other: Administration of patient self-assessment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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