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Customized Contact Lenses

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University of Houston

Status

Not yet enrolling

Conditions

Keratoconus

Treatments

Device: Customized contact lens

Study type

Interventional

Funder types

Other

Identifiers

NCT05134909
STUDY00003195

Details and patient eligibility

About

The overall goal of this project is to improve the visual quality of individuals who have abnormal corneal conditions that alter the shape of their cornea (eg. keratoconus). Patients with an abnormal corneal shape have substantial lower and higher order aberrations (distortions in the eye). This results in reduced visual acuity which cannot be corrected by regular sphero-cylindrical correction. Compensating for these aberrations has been challenging due to difficulty measuring their wavefront aberrations accurately and, consequently, manufacturing the custom contact lenses with irregular optical profiles. This project is designed to systematically overcome these obstacles with a customized scleral and/or soft contact lens capable of compensating for the lower and higher order aberrations of the eye.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Able to read and understand the informed consent document in English
  • 18 to 75 years of age
  • Received diagnosis of keratoconus by a clinician
  • Willing and able to follow instructions

Exclusion criteria

  • Has best corrected visual acuity of 20/20 or better in the keratoconic eye(s).
  • Normal/typical subjects
  • Is unable to handle, insert, remove or care for the study lenses.
  • Has any active anterior segment disease, pathology, or surgery affecting vision, refraction, or the ability to wear a contact lens
  • History of ocular pharmacological treatment
  • History of ocular trauma or surgery causing abnormal corneal curvature or distorted vision History of contact lens intolerance
  • Pregnant at the time of enrollment in the study (self-reported- It has been shown hormonal changes during pregnancy may affect corneal biomechanics negatively)
  • Adults unable to consent
  • Individuals who are not yet adults (infants, children, teenagers under the age of 18 because it has been shown the average age of the appearance of Keratoconus is the second decade of life ( 15-18 years of age)
  • Prisoners

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

60 participants in 1 patient group

Study: Keratoconus
Experimental group
Description:
Customized contact lenses will be fitted to each study subject based on their own optical defects.
Treatment:
Device: Customized contact lens

Trial contacts and locations

0

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Central trial contact

Ayeswarya Ravikumar, PhD; Geunyoung Yoon, PhD

Data sourced from clinicaltrials.gov

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