Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01489501

Multicenter Study of CAOMECS Transplantation to Patients With Total Limbal Stem Cell Deficiency

Multicenter Study of Cultured Autologous Oral Mucosal Epithelial Cell-Sheet (CAOMECS) Transplantation to Patients With Total Limbal Stem Cell Deficiency

Status
Withdrawn
Phase
Phase 3
Study type
Interventional
Enrollment
0 (actual)
Sponsor
CellSeed France S.A.R.L. · Industry
Sex
All
Age
2 Years – 74 Years
Healthy volunteers
Not accepted

Summary

This clinical study is a scientific study on patients who do not have any limbal stem cells. In this clinical study tissue is taken from the inside of the mouth, and cells from that tissue (epithelial cells) will be grown to form a multilayered cell-sheet, called CAOMECS, which is then transplanted onto the cornea. This transplantation method should repair the damage of the cornea. The aim of this study is to see if the transplantation of CAOMECS renews the surface of the eye, by preventing the growth of the conjunctiva over the cornea and stopping new small blood vessels forming.

Detailed description

This is an open clinical study without a control group, which means that all patients will be given the study treatment (CAOMECS). Adults as well as minor patients can participate in this clinical trial. CAOMECS is undergoing a clinical trial, which means that it has not yet been officially approved for the treatment of this disease. Up to now it was clinically tested in France, on 26 people with limbal stem cell loss. Study objective The objective of this study is to restore the ocular surface epithelium of patients with total LSCD by preventing or reducing recurrent conjunctivalization and neovascularization up to 12 months post-transplantation. Methodology This is a prospective, open, multi-center study with CAOMECS in patients with total LSCD. Stem cells will be isolated from an oral mucosa biopsy and will be grown in cell culture. The resultant epithelial cell-sheets will then be transplanted to the ocular surface of the respective patients under general anesthesia. After transplantation patients may be hospitalized according to routine clinical practice. Overall, the study will consist of a screening visit where eligibility will be evaluated, the day of the biopsy, the day before the transplantation where baseline data will be evaluated, the transplantation (day 0), and a follow-up period consisting of nine visits at days 1, 5, and 10 and months 1, 3, 6, 12, 24, and 36. Other visits as clinically indicated may also occur.

Conditions

Interventions

TypeNameDescription
PROCEDURESurgical transplantation of CAOMECS to the ocular surfaceSurgical transplantation of oral mucosa derived CAOMECS sheet onto eye cornea.

Timeline

First posted
2011-12-09
Last updated
2015-03-25

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT01489501. Inclusion in this directory is not an endorsement.