CLET-4-LSCD: Cultivated Limbal Epithelial Transplantation (CLET) for Limbal Stem Cell Deficiency (LSCD)

Sponsor
Instituto Universitario de Oftalmobiología Aplicada (Institute of Applied Ophthalmobiology) - IOBA (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT03884569
Collaborator
Citospin (Industry), Red de Terapia Celular (Industry), University of Valladolid (Other)
30
1
9
3.3

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    30 participants
    Observational Model:
    Cohort
    Time Perspective:
    Other
    Official Title:
    Cultivated Limbal Epithelial Transplantation (CLET) for Limbal Stem Cell Deficiency (LSCD): an Observational Study on Safety and Effectiveness
    Anticipated Study Start Date :
    Apr 1, 2022
    Anticipated Primary Completion Date :
    Dec 31, 2022
    Anticipated Study Completion Date :
    Dec 31, 2022

    Arms and Interventions

    Arm Intervention/Treatment
    Patients treated with CLET

    Previously treated with CLET patients are included retrospectively, as the follow-up procedure is already stablished in our centre, and patients treated following standard care or through "drugs-in-special-situation" request in Spain prospectively. Patients are not treated to be included in the study, only the follow-up variables are taken into account.

    Outcome Measures

    Primary Outcome Measures

    1. 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.

    2. 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.

    3. 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.

    4. 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.

    5. Percentage of improvement in corneal conjunctivalization [6 months]

      Percentage of corneal area with conjunctivalization (superficial opacity and/or superficial neovascularization) will be measured.

    6. Complete absence of persistent epithelial defects [6 months]

      Corneal fluorescein staining has to rule out epithelial breakdown

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No

    Total and/or severe LSCD of any etiology in one or both eyes.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 IOBA Valladolid Spain 47011

    Sponsors and Collaborators

    • Instituto Universitario de Oftalmobiología Aplicada (Institute of Applied Ophthalmobiology) - IOBA
    • Citospin
    • Red de Terapia Celular
    • University of Valladolid

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Instituto Universitario de Oftalmobiología Aplicada (Institute of Applied Ophthalmobiology) - IOBA
    ClinicalTrials.gov Identifier:
    NCT03884569
    Other Study ID Numbers:
    • IOBA201901
    First Posted:
    Mar 21, 2019
    Last Update Posted:
    Feb 7, 2022
    Last Verified:
    Feb 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Instituto Universitario de Oftalmobiología Aplicada (Institute of Applied Ophthalmobiology) - IOBA

    Study Results

    No Results Posted as of Feb 7, 2022