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Comparison of Three Different No-contact Pachymetries

U

University of Catanzaro

Status

Unknown

Conditions

Corneal Thickness

Treatments

Device: Pachymetry

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Study wants to compare central corneal thickness (CCT) obtained through 3 different no-contact instruments and to compare them with contact ultrasound pachymetry, actually the gold standard technique.

Full description

Corneal pachymetry is the measurement of corneal thickness, usually expressed in microns (μ).

Pachymetry is systematically used for the monitoring of corneal oedema, for the management and assessment of the progression risk of the ocular hypertension, for the diagnosis, the management and follow-up of keratoconus, as well as it is important in the pre and postoperative management of corneal surgical procedures. CCT is a factor well known to influence tonometry. Its assessment is fundamental in glaucoma practice to allow a correct intraocular pressure (IOP) evaluation.

The purpose of this study is to compare CCT measurements using four different instruments: Scheimpflug camera tomography, spectral-domain optical coherence tomography (SD-OCT), anterior chamber SD-OCT and ultrasound pachymetry.

Enrollment

150 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • subjects that gave a valid consensus to be included in this experimentation,
  • aged between 18 and 75 years,
  • Best-Corrected Visual Acuity (BCVA) of 20/100 or better,
  • refraction included between -6 and +6 dioptres,
  • astigmatism included between -2 and +2 dioptres.

Exclusion criteria

  • History of refractive surgery or any keratoplasty procedure,
  • corneal opacities or diseases that make not suitable applanation tonometry or pachymetry.
  • Use of contact lenses.
  • History of corneal dystrophies or degenerative diseases, (like keratoconus and pellucid marginal degeneration).
  • History of glaucoma or ocular hypertension.

Trial design

150 participants in 1 patient group

Pachymetry
Description:
All recruited volunteers in present study, that underwent pachymetry measurement with four different instruments
Treatment:
Device: Pachymetry

Trial contacts and locations

1

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Central trial contact

Luigi Varano, M. D.; Giovanni Scorcia, M. D.

Data sourced from clinicaltrials.gov

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