Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID05400590

Comparison of the Healing Properties on Corneal Cells of Growth Factor-Enriched Plasma and Autologous Serum From Aniridia Patients

Led by Fondation Ophtalmologique Adolphe de Rothschild · Updated on 2025-12-08

24

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying the healing and anti-fibrotic effects of two blood-derived products, autologous serum and growth factor-rich plasma, on corneal cells from patients with aniridia compared to healthy controls. Aniridia causes abnormal corneal healing leading to scarring and clouding, and while autologous serum aids healing, it does not prevent fibrosis. This study aims to compare these two products' effects in the lab, examining their potential to reduce fibrosis markers. Participants include patients with aniridia and healthy controls. Blood samples are collected from all participants, with half used to prepare autologous serum and the other half to prepare growth factor-rich plasma for laboratory testing. Additionally, a conjunctival impression, a minimally invasive procedure collecting superficial eye surface cells, is performed at enrollment for biological analysis. Participants will have blood drawn and conjunctival samples collected at the start. Researchers will compare how the blood products affect corneal cell healing and fibrosis markers in vitro. The study monitors these laboratory outcomes to understand differences between aniridia patients and controls. The total participation involves these baseline collections and laboratory evaluations without further interventions or treatments.

CONDITIONS

Brief Title

Comparison of the Healing Properties on Corneal Cells of Groth Factor-enriched Plasma and Autologous Serum From Aniridia Patients

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • For patients with aniridia: diagnosed with aniridia
  • Weight over 43 kilograms
  • If treated with autologous serum, at least 8 weeks since last blood collection
  • If blood donation was made, at least 8 weeks since last donation
  • For controls: no signs of aniridia
  • Weight over 43 kilograms
  • Matched to a case for sex and age within 10 years
  • No known diabetes
  • If blood donation was made, at least 8 weeks since last donation
Not Eligible

You will not qualify if you...

  • Insufficient sample volume
  • No conjunctival impression collected
  • Positive for HBV, HCV, or HIV serology
  • For aniridia cases, no genetic confirmation of aniridia

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Sample Collection

Duration - 1 day

Participants provide blood samples and undergo conjunctival impression collection for biological analysis of ocular surface diseases.

1 visit (in-person)

In Vitro Analysis

Duration - Duration of laboratory analysis

Collected samples are used to compare the healing properties of autologous serum and growth factor-enriched plasma on corneal cells in a laboratory setting.

No participant visits required

Trial Site Locations

Total: 1 location

1

Hôpital Fondation A. de Rothschild

Paris, France, 75019

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Research Team

A

Amélie YAVCHITZ

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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