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Search / Trial NCT01234207

Clinical Assessment of a Customized Free-form Progressive Addition Lens Spectacle

Launched by UNIVERSITY OF CALIFORNIA, BERKELEY · Nov 3, 2010

Trial Information

Current as of July 23, 2025

Completed

Keywords

Progressive Addition Lenses Customized Free Form Presbyopia Bifocals Subjective Assessment Visual Performance Visual Acuity Amsler Grid

ClinConnect Summary

In a double-masked crossover trial, 95 experienced wearers wore customized free-form PAL spectacles (Test) and standard non-free-form PAL spectacles (Control) for one week each. All subjects wore both Test and Control spectacles, and the pair to be worn first was randomly assigned. At dispensing and after 1 week of wear, subjects were tested for distance and near visual acuity (VA) under both high and low contrast; in addition, 30 degree off-axis VA was measured using a novel apparatus, as was the horizontal extent of undistorted vision at reading distance. Subjects also completed a set of ...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Presbyope
  • Experienced PAL spectacle wearer
  • Correctable to at least 20/25 in both eyes
  • Able and willing to use Test and Control spectacles for 1 week each as primary form of presbyopia correction
  • Able and willing to complete all laboratory measurements and questionnaire batteries
  • Exclusion Criteria:
  • Purchasing free-form PAL spectacles from the UC Berkeley Eyewear Center
  • Having eye conditions or diseases that could potentially cause a decrease in visual acuity over the course of participation in the study
  • Having eye conditions or diseases that could potentially interfere with ability to use Test and Control spectacles as primary form of presbyopia correction

About University Of California, Berkeley

The University of California, Berkeley, a leading research institution renowned for its commitment to scientific innovation and academic excellence, serves as a prominent sponsor of clinical trials aimed at advancing medical knowledge and improving patient outcomes. With a robust infrastructure for interdisciplinary collaboration, UC Berkeley leverages its distinguished faculty, cutting-edge laboratories, and extensive resources to conduct research that addresses critical health challenges. The university is dedicated to fostering a culture of ethical research practices and ensuring the highest standards of safety and efficacy in its clinical investigations, ultimately contributing to the translation of scientific discoveries into tangible health solutions.

Locations

Berkeley, California, United States

Patients applied

0 patients applied

Trial Officials

Meng C. Lin, OD, PhD

Principal Investigator

Clinical Research Center, School of Optometry, University of California, Berkeley

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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