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Contact Lenses and Infiltrative Keratitis (CLIK)

S

State University of New York College of Optometry

Status

Completed

Conditions

Keratitis

Treatments

Device: senofilcon A

Study type

Interventional

Funder types

Other

Identifiers

NCT02186431
CLIK_601933

Details and patient eligibility

About

To quantify and compare baseline tear proteins and ocular response in contact lens wearers with a history of corneal infiltrative events, to those without a history of complications. This will be accomplished via measurement of select anti-inflammatory tear proteins before, during and after contact lens wear.

Enrollment

32 patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Soft contact lens wearers
  • Healthy (control), or with history of infiltrative keratitis (case)
  • Has a wearable pair of glasses
  • Refractive error between +8.00 D and -12.00 D, with less than 1.50 D of astigmatism

Exclusion criteria

  • Smoker
  • Pregnant or nursing
  • Systemic disease that would effect tear proteins
  • Punctal plugs
  • Use of eye drops in the last week

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

32 participants in 2 patient groups

history of corneal infiltrative events
Experimental group
Description:
To quantify and compare baseline tear proteins and ocular response in contact lens wearers with a history of corneal infiltrative events
Treatment:
Device: senofilcon A
without a history of corneal infiltrative events
Active Comparator group
Description:
To quantify and compare baseline tear proteins and ocular response in contact lens wearers without a history of corneal infiltrative events.
Treatment:
Device: senofilcon A

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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