Corneal Epithelial Dystrophy
Conditions
Keywords
Tissue-Cultured Human Amniotic Epithelial Cells onto damaged corneal surface
Brief summary
To investigate the effect of using tissue cultured human amniotic epithelial cells to re-establish severely damaged ocular surfaces. Specifically, to determine the efficacy of transplanted tissue cultured amniotic epithelial cells on persistent corneal epithelial defect, a potential visual threaten ocular disorder.
Detailed description
Ocular surface diseases and injury caused by chemicals, result in chronic ulceration, and may never be able to be healed normally, and may lead to permanent vision loss. Standard medical treatments often fail. Histologically and somehow functionally, human amniotic cells are similar to ocular surface cells, and these cells have been shown to be safe to be transplanted to another subject and will not be rejected by the recipient. In animal studies, amniotic cells demonstrated that they can re-establish the integrity of ocular surface in more than 30% of recipients without apparent toxic side effects. This study will investigate this novel strategy for its effect on human ocular surface disorder. It will provide a potential alternative therapy for this difficult and devastating disease.
Interventions
PROCEDURETransplantation of Tissue-Cultured Human Amniotic Epithelial Cells
Sponsors
University of Texas Southwestern Medical Center
Study design
Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 88 Years
Healthy volunteers
Yes
Inclusion criteria
* Patients with corneal epithelial defects and ulcers that have persisted for 4 weeks or longer, regardless of their cause. These patients will have received traditional medical therapy, including correcting the underlying causes, suppressing inflammation, and augmenting the tissue healing processes, but the epithelial defects have persisted.
Exclusion criteria
* Patients who are pregnant or under age 18 will be excluded. * Placentas will not be used if the following problems are present: * If the mother has an infection at the time of her baby's birth; * If the mother has a high risk of developing infection due to intravenous drug use or other factors; * If the mother has diabetes, arthritis, or raised blood pressure; * If the baby is unhealthy; * If there is evidence of infection of the womb (uterus) and afterbirth (placenta) at the time of delivery.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Ocular surface healing | 30 days following initiation of treatment |
Countries
United States
Outcome results
None listed