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CompletedNCT07194538KCXL-1YUpdated Oct 1, 2025

One-Year Outcomes After Conventional vs Accelerated Epi-Off Corneal Cross-Linking in Progressive Keratoconus (Observational Cohort)

An observational study in Keratoconus, sponsored by Clinical Hospital Centre Zagreb. Completed at 1 site in Croatia. Per ClinicalTrials.gov, last updated 2025-10-01.

Sponsored by Clinical Hospital Centre Zagreb · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
20
Sex
All
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Study summary

Prospective, observational (consecutive eligible eyes) continuation of a previously published 6-month cohort from the same center, extending follow-up to 12 months. Patients with progressive keratoconus received either conventional (CXL30: 3 mW/cm² × 30 min) or accelerated (CXL10: 9 mW/cm² × 10 min) epi-off CXL as part of routine clinical care. Assignment to CXL30 or CXL10 was at the discretion of the treating surgeon; no prospective allocation or randomization was performed. Outcomes included ABCD grading metrics (ABCD-A/B), Kmax, anterior/posterior radii of curvature (ARC/PRC), thinnest pachymetry, and visual acuity at 12 months. The primary objective was to evaluate one-year stabilization/remodeling and compare anterior/posterior responses between protocols.

Read the detailed description

This prospective, single-center observational cohort extends the follow-up of a previously reported 6-month series from the same center to a 12-month horizon. The study population comprises consecutive patients with progressive keratoconus managed with standard-of-care, epi-off corneal collagen cross-linking (CXL) at the University Hospital Centre Zagreb. Patients were treated according to routine clinical decision-making by the attending surgeon; no prospective allocation or randomization to a protocol was performed. In routine care, some eyes underwent conventional CXL30 (Dresden-type; UVA 370 nm, 3 mW/cm² for 30 min) and others underwent CXL10 (accelerated; UVA 370 nm, 9 mW/cm² for 10 min). Riboflavin 0.1% solution was used per institutional practice. All procedures were epi-off.

Rationale. While both conventional and accelerated CXL are widely used in daily practice, comparative one-year data that integrate tomographic metrics from the ABCD grading system with traditional surrogates (e.g., Kmax) help clarify the balance between anterior corneal flattening, posterior remodeling, and pachymetric behavior under real-world conditions. This observational design captures effectiveness and safety without altering clinical decision pathways.

Design and cohorts. Consecutive eligible eyes were enrolled at the time of surgery and followed prospectively at baseline (day of surgery) and 1, 3, 6, and 12 months. Two observational cohorts are defined post hoc by the protocol actually received in standard care:

CXL30 (Conventional): continuous UVA 3 mW/cm² × 30 min (Dresden-type).

CXL10 (Accelerated): continuous UVA 9 mW/cm² × 10 min.

Assignment to CXL30 vs CXL10 was at the surgeon's discretion based on routine clinical considerations; the study did not prospectively assign interventions.

Eligibility. Inclusion required progressive keratoconus documented on serial Scheimpflug tomography within the prior 12 months; a clear corneal axis (no visually significant scarring); and corneal thickness 370 µm or more per institutional safety protocol. Exclusions comprised no central corneal scars, prior chemical burns, severe corneal infection, or ocular surface disease. Pregnancy and lactation during treatment were also contraindications.

Examinations and outcomes. Outcomes were assessed using Scheimpflug tomography (e.g., Pentacam or equivalent) and standard visual testing. The primary outcome was change in ABCD-A (anterior corneal curvature metric) from baseline to 12 months. Secondary outcomes included Kmax, anterior and posterior radii of curvature (ARC/PRC), thinnest pachymetry, and UDVA/BCVA at 12 months. Safety endpoints encompassed delayed epithelial healing (>7 days), infectious keratitis, clinically significant corneal haze, endothelial decompensation, and need for re-treatment.

Follow-up timeline. Enrollment/treatment occurred May 2021-December 2021; 12-month follow-up was completed by January 2023. Of the 28 eyes in the previously reported 6-month cohort, 22 completed the 12-month visit and were included in this analysis.

Data handling and oversight. Data were collected prospectively in a standardized fashion and analyzed as observational (no masking, no allocation). The protocol was reviewed and approved by the institutional Ethics Committee; all analyses used de-identified data. No data monitoring committee was required given the non-interventional, standard-of-care nature of the study.

Statistical approach (summary). Effectiveness outcomes are summarized descriptively; within-cohort change from baseline to 12 months is evaluated with paired tests on continuous variables as appropriate to distributional assumptions. Between-cohort comparisons (CXL30 vs CXL10) at 12 months and for change scores are explored with two-sample tests or generalized linear models with adjustment for prespecified covariates (e.g., baseline severity indices) where applicable. Statistical significance is assessed at a two-sided α = 0.05, with corresponding confidence intervals to aid interpretation.

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Conditions studied

  • Keratoconus

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Keywords

  • keratoconus
  • corneal crosslinking
  • conventional CXL
  • accelerated CXL
  • ABCD grading system
  • one-year outcome
  • Scheimpflug tomography
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In context

Keratoconus

307 studies on the registry are indexed under Keratoconus; 56 are open to participants now.

This study's enrollment of 20 is below the median of 130 across 94 observational studies indexed under Keratoconus.

Browse Keratoconus studies →

Lead sponsor

Clinical Hospital Centre Zagreb is the lead sponsor of 31 studies on the registry; 9 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with progressive keratoconus treated at University Hospital Centre Zagreb (Croatia).

Inclusion criteria

  • Progressive keratoconus documented on serial Scheimpflug tomography within the prior 12 months (ABCD/K-metrics and/or pachymetry).
  • Clear corneal axis (no visually significant scarring).
  • Corneal thickness 370 μm or more

Exclusion criteria

Exclusion Criteria:

  • No central corneal scars, prior chemical burns, severe corneal infection, or ocular surface disease.
  • No pregnancy and lactation during treatment.
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
20 participants (actual)
Patient registry
No

Groups and cohorts

  • Cohort 1 - CXL30 (Conventional)

    Conventional Dresden protocol; irradiance 3 mW/cm² for 30 minutes; epi-off; riboflavin 0.1%. Assignment was per treating surgeon's standard-of-care decision (no prospective allocation).

  • Cohort 2 - CXL10 (Accelerated)

    Accelerated protocol; irradiance 9 mW/cm² for 10 minutes; epi-off; riboflavin 0.1%. Assignment was per treating surgeon's standard-of-care decision (no prospective allocation).

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What researchers measure

Primary outcomes

  1. Change in ABCD-A from baseline to 12 months

    Belin ABCD parameter A = A stage (ordinal severity stage); Belin ABCD keratoconus grading system (A = anterior corneal radius of curvature at the thinnest point; B = posterior corneal radius of curvature at the thinnest point; C = thinnest corneal pachymetry; D = distance best-corrected visual acuity). minimum value 0, maximum value 4 (ordinal scale 0-4) higher score means worse outcome

    Time frame: 12 months

Secondary outcomes

  1. Change in ARC from baseline to 12 months

    ABCD A = ARC; mm ARC - anterior radius curvature calculated from a 3.0 mm optical zone centered on the thinnest point of the cornea higher = flatter (better); mm

    Time frame: 12 months

  2. Change in PRC from baseline to 12 months

    PRC; mm PRC - posterior radius curvature calculated from a 3.0 mm optical zone centered on the thinnest point of the cornea higher = flatter (better); mm Time Frame: 12 months

    Time frame: 12 months

  3. Change in Kmax from baseline to 12 months

    Time frame: 12 months

  4. Change in UDVA and BCVA from baseline to 12 months

    UDVA = uncorrected visual acuity ; BVCA = best corrected visual acuity

    Time frame: 12 months

  5. Change in thinnest pachymetry from baseline to 12 months

    Time frame: 12 months

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Study locations

1 site
  • University Hospital Centre Zagreb
    Zagreb, 10 000, Croatia
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References and documents

Individual participant data

Plan to share: No — Individual participant datasets will not be shared. The informed consent and IRB approval did not include permission for public sharing of participant-level data, and the small, single-center cohort with imaging-derived variables carries a residual re-identification risk. De-identified aggregate results and summary tables will be available in the published article and can be provided upon reasonable request to the corresponding author, subject to institutional approvals.

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 1, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07194538
Lead sponsor
Clinical Hospital Centre Zagreb
Responsible party
Iva Bešlić (Medical Doctor, Ophtalmology and Optometrist Specialist, FEBO, Clinical Hospital Centre Zagreb) — Principal investigator
First posted
Sep 26, 2025
Start date
May 9, 2021
Primary completion
Jan 12, 2023
Completion
Jan 12, 2023
Last update
Oct 1, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Sep 2025. You cannot join it, but the record below documents what was studied.

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