NCT06265298

Brief Summary

Objectives The transparent surface of the eye, called the cornea, plays a crucial role in transmitting light to the retina and in protecting the eye. On its external surface, the cornea is composed of a constantly renewing multistratified epithelium. This mechanism is fueled by stem cells located in the limbus (the transition zone between the cornea and the sclera). Limbal Stem Cell Deficiency (LSCD) is characterized by a decrease or cessation of epithelial renewal and neovascularization of the cornea. Consequently, the cornea loses its integrity and transparency. This visually impairing condition is currently in a therapeutic impasse as only autologous limbal or allogeneic corneal grafts are viable options, but they pose significant risks to patients. Studies have shown that the oral cavity contains stem cells that can be isolated, cultured, and transdifferentiated into limbal stem cells (LSCs). However, to date, these studies are limited, and no protocol has been validated. In this study, the advantage of the accessibility of the oral cavity is used to develop a protocol for differentiating cells from the oral mucosa into limbal stem cells (LSCs) for use in a future clinical trial with patients. Methodology This prospective monocentric study will be conducted on patients from the ophthalmology department of the Montpellier University Hospital who have an indication for conjunctival reconstruction. After obtaining consent from the patients, cells from the oral wall will be sent to the tissue bank of the Montpellier University Hospital, where they will be cultured. Finally, the transdifferentiation steps will be analyzed by the "Eye" research team at the Institute of Neuroscience in Montpellier, which is collaborating on the project. The investigators have established objective factors to assess the success of the developed protocol based on the literature : (i) \> 3% of stem cells in primary cultures, (ii) \<10% aborted colonies, (iii) Expression of LSC markers (Pax6, Krt14, p63).

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
4

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jun 2024

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 24, 2024

Completed
27 days until next milestone

First Posted

Study publicly available on registry

February 20, 2024

Completed
4 months until next milestone

Study Start

First participant enrolled

June 19, 2024

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2025

Completed
Last Updated

August 19, 2024

Status Verified

August 1, 2024

Enrollment Period

12 months

First QC Date

January 24, 2024

Last Update Submit

August 16, 2024

Conditions

Keywords

epitheliummucosacorneacorneal epithelium

Outcome Measures

Primary Outcomes (5)

  • Successful Transdifferentiation

    Successful differentiation, defined by the percentage of stem cells on primary cultures ≥ 3%

    change over time between Baseline and 14 days

  • Successful Transdifferentiation

    Successful differentiation, defined by the percentage of aborted colonies \< 10%.

    change over time between Baseline and 14 days

  • Successful Transdifferentiation

    The quantitative real-time polymerase chain reaction, (qPCR) technique will be used to monitor expression levels of limbal stem cell markers such as Krt14 and Krt5. The qPCR technique will be used to monitor expression levels of transcription factors.

    change over time between Baseline and 14 days

  • Successful Transdifferentiation

    Successful differentiation, defined by the presence of transcription factors p63 and Pax6 The qPCR technique will be used to monitor expression levels of transcription factors.

    change over time between Baseline and 14 days

  • Successful Transdifferentiation

    The qPCR technique will be used wiil be used to monitor the absence of expression of markers of terminal differentiation of corneal epithelial cells, such as Krt3 and Krt12

    change over time between Baseline and 14 days

Study Arms (1)

Reconstruction conjonctival

EXPERIMENTAL

Patients undergoing conjunctival reconstruction using oral mucosa

Procedure: Conjunctival reconstruction

Interventions

Conjunctival reconstruction using buccal mucosa taken from the patient's mouth. Following the reconstruction operation, an additional biopsy of buccal mucosa will be taken to develop a laboratory protocol for the transdifferentiation of these buccal cells into corneal epithelial stem cells.

Reconstruction conjonctival

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Presenting an indication for conjunctival reconstruction using oral mucosa (for example because of a recurrent pterygium, conjunctival carcinoma or ocular burn)
  • Written consent to participate in this research

You may not qualify if:

  • Chronic infection (HIV, hepatitis, tuberculosis, Lyme disease)
  • Oral pathology which could affect the health of the oral mucosa tissue according to the opinion of the investigating doctor
  • Uncontrolled systemic disease
  • Pregnant or breastfeeding

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHU Gui de Chauliac - Service d'Ophtamologie

Montpellier, Occitanie, 34295, France

RECRUITING

MeSH Terms

Conditions

Limbal Stem Cell DeficiencyCorneal Diseases

Condition Hierarchy (Ancestors)

Eye Diseases

Study Officials

  • Vincent Daien, MD PhD

    v-daien@chu-montpellier.fr

    STUDY DIRECTOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
OTHER
Intervention Model
SINGLE GROUP
Model Details: transversal and fundamental study
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 24, 2024

First Posted

February 20, 2024

Study Start

June 19, 2024

Primary Completion

June 1, 2025

Study Completion

June 1, 2025

Last Updated

August 19, 2024

Record last verified: 2024-08

Data Sharing

IPD Sharing
Will not share

Locations