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Starting soon Observational

Cultivated Limbal Epithelial Transplantation (CLET) for Limbal Stem Cell Deficiency (LSCD)

NCT03884569 · tracked via the Priya Life Science Spain tracker
Phase
Observational
Started
2025-11
Last updated
2025-05-16

Condition(s) studied

Limbal Stem-cell Deficiency

Study summary

CLET is a published treatment for the management of corneal failure due to extensive LSCD. Due to our previous studies on this novel treatment, the regulatory agency of Spain "Agencia Española de Medicamentos y Productos Sanitarios (AEMPS)" authorized our institution (IOBA-University of Valladolid) to perform this kind of therapy (CLET) in a case-by-case base following the Special Situation Medicines Policy Procedure in Spain. Upon approval of the permanent authorization patients will be included as specified by AEMPS.The objective of this study is to perform a protocolized treatment and follow up so that results can be reported to the scientific community.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Total and/or severe LSCD of any etiology in one or both eyes.

Primary outcome measure(s)

  • Points of improvement in the Single Item Dry Eye Questionnaire (SIDEQ) — 6 months
    The SIDEQ gives a 0-4 score about the presence of dryness, foreign body sensation, burning/stinging, pain, itching, sensitivity to light, and blurred vision, where higher scores indicate higher intensity of the symptom (maximun score: 28). One of the primary outcomes for this work is the improvement in any of the four questionnaires shown here.
  • Points of improvement about the Ocular Surface Disease Index (OSDI) — 6 months
    The OSDI evaluates ocular surface symptoms with 12 questions, and scores \>12 indicate abnormal symptomatology, and \>32 means severe symptoms (maximum score 100). One of the primary outcomes for this work is the improvement in any of the four questionnaires shown here.
  • Points of improvement in the National Eye Institute 25-item Visual Function Questionnaire (NEI-VFQ25) — 6 months
    The visual function-related aspects of the quality of life were evaluated with the NEI-VFQ25, where higher scores on a 0 to 100 scale indicate better function. One of the primary outcomes for this work is the improvement in any of the four questionnaires shown here.
  • Points of improvement in the Change in Dry Eye Symptoms Questionnaire (CDES-Q) — 6 months
    The CDES-Q evaluates ocular surface symptoms with two questions, CDES-Q1 and CDES-Q2. CDES-Q1 evaluates the change in symptoms occured since the previous examination (same, better or worse). CDES-Q2 evaluates the magnitude of the change in a scale from 0 to 10, where 0 means "slightly better/worse" and 10 means "extremely better/worse". One of the primary outcomes for this work is the improvement in any of the four questionnaires shown here.
  • Percentage of improvement in corneal conjunctivalization — 6 months
    Percentage of corneal area with conjunctivalization (superficial opacity and/or superficial neovascularization) will be measured.
  • Complete absence of persistent epithelial defects — 6 months
    Corneal fluorescein staining has to rule out epithelial breakdown

Trial sites (1)

FacilityCityRegionStatus
IOBA Valladolid Spain

More Instituto Universitario de Oftalmobiología Aplicada (Institute of Applied Ophthalmobiology) - IOBA trials in Spain

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03884569 on ClinicalTrials.gov ↗ ← All trials in Spain