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Safety & Effectiveness of the PXL-Platinum 330 System for CXL Using Riboflavin Solution

C

Cornea Associates of Texas

Status and phase

Completed
Phase 1

Conditions

Keratoconus
Pellucid Marginal Corneal Degeneration
Corneal Ectasia
Corneal Degeneration

Treatments

Combination Product: PXL-330 Platinum device for crosslinking with Peschke riboflavin solution

Study type

Interventional

Funder types

Other

Identifiers

NCT04667572
PXL-330-CAT-2

Details and patient eligibility

About

Safety and Effectiveness of the PXL-Platinum 330 System for Corneal Collagen Cross-linking in Eyes With Corneal Thinning Conditions

Full description

Patients with progressive keratoconus, pellucid marginal degeneration, or at risk for post-refractive corneal ectasia will be recruited and undergo epithelial-on corneal crosslinking with the Peschke PXL-330 system using pulsed, accelerated energy delivery. Patients will undergo monitoring for 1 year, with serial measurements of corneal topography, visual acuity, pachymetry, and visual function.

Enrollment

249 patients

Sex

All

Ages

8+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 8 years of age or older
  • Signed written informed consent
  • Willingness and ability to comply with schedule for follow-up visits
  • Contact Lens Wearers Only:
  • Removal of contact lenses (if applicable) for the required period of time prior to the screening refraction: Soft, discontinue 3 days; Soft Extended Wear, discontinue 3 days; Soft Toric, discontinue 3 days; Rigid gas permeable, discontinue 2 Weeks (subjects who cannot function without wearing their contact lenses, may forgo discontinuation of contact lenses)

And one or more of the following:

  • Presence of central or inferior steepening.
  • Axial topography consistent with keratoconus, post-surgical ectasia, or pellucid marginal degeneration
  • Presence of one or more findings associated with keratoconus or pellucid marginal degeneration, such as: Fleischer ring, Vogt's striae, Decentered corneal apex, Munson's sign, Rizzutti's sign, Apical Corneal scarring consistent with Bowman's breaks, Scissoring of the retinoscopic reflex, Crab-claw appearance on topography
  • Steepest keratometry (Kmax) value ≥ 47.20 D
  • I-S keratometry difference > 1.5 D on the Pentacam/Orbscan map or topography map
  • Posterior corneal elevation >16 microns
  • Thinnest corneal point >300 microns

Exclusion criteria

  • Eyes classified as either normal or atypical normal on the severity grading scheme.
  • Corneal thickness < 300 microns measured by ultrasonic pachymetry or pentacam.
  • Previous ocular condition (other than refractive error) in the eye(s) to be treated that may predispose the eye for future complications, for example: History of or active corneal disease (e.g., herpes simplex, herpes zoster keratitis, recurrent erosion syndrome, etc.) Clinically significant corneal scarring in the CXL treatment zone that is not related to keratoconus or, in the investigator's opinion, will interfere with the cross-linking procedure.
  • Pregnancy (including plan to become pregnant) or lactation during the course of the study
  • A known sensitivity to study medications
  • Patients with nystagmus or any other condition that would prevent a steady gaze during the CXL treatment or other diagnostic tests.
  • Patients with a current condition that, in the physician's opinion, would interfere with or prolong epithelial healing

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

249 participants in 2 patient groups

Pulsed 5mW/cm2
Experimental group
Description:
5mW/cm2, with pulsed mode, 10 seconds on, 10 second off, for 36 minute total treatment time
Treatment:
Combination Product: PXL-330 Platinum device for crosslinking with Peschke riboflavin solution
Pulsed 8mW/cm2
Experimental group
Description:
8mW/cm2, with pulsed mode, 10 seconds on, 10 second off, for 22 minute and 30 seconds total treatment time
Treatment:
Combination Product: PXL-330 Platinum device for crosslinking with Peschke riboflavin solution

Trial contacts and locations

1

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Central trial contact

Jennifer Seale, COT; Tyrone McCall, MD

Data sourced from clinicaltrials.gov

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