Comparison of the Healing Properties on Corneal Cells of Groth Factor-enriched Plasma and Autologous Serum From Aniridia Patients
Fondation Ophtalmologique Adolphe de Rothschild
24 participants
May 15, 2023
OBSERVATIONAL
Conditions
Summary
Keratopathy of patients with aniridia leads to epithelial scarring disorders and a progressive clouding of the cornea linked to this abnormal healing (fibrosis). Treatment with autologous serum is usually undertaken to promote epithelial healing. However, autologous serum does not prevent the formation of fibrosis, whereas growth factor-rich plasma appears to be associated with a reduction in the in vitro expression of fibrosis markers. This study seeks to compare the in vitro healing and anti-fibrotic properties of autologous serum and growth factor rich plasma from aniridia patients and healthy controls.
Eligibility
Inclusion Criteria11
- For patients with aniridia:
- With aniridia
- Patient weighing more than 43 kg
- If the patient is being treated with autologous serum, a delay of 8 weeks after the last blood collection
- If a blood donation has been made, a delay of 8 weeks must be respected after the last donation
- For controls:
- Non-aniridia (no clinical signs)
- Weighing more than 43 kg
- Matched to a case for sex and age +/-10 years
- No known diabetes
- If a blood donation has been made, a delay of 8 weeks must be respected after the latter
Exclusion Criteria4
- Insufficient sample volume
- No conjunctival print
- HBV, HCV, HIV serology positive
- Aniridia not genetically confirmed for cases For each patient excluded, a new patient will be included in order to maintain the number of patients required for data analysis.
Interested in this trial?
Get notified about updates and connect with the research team.
Interventions
2.5% of body weight
Collection of the most superficial conjunctival epithelial cells (desquamating) in a non- or minimally invasive, quick and almost painless way, for a biological analysis of ocular surface diseases. Application of a filter paper on the bulbar conjunctiva, under local anesthesia.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT05400590