Safety and Efficacy of Subretinal Transplantation of Clinical Human Embryonic Stem Cell Derived Retinal Pigment Epitheliums in Treatment of Retinitis Pigmentosa
Condition(s) studied
Investigational drug(s) / intervention(s)
Retinal pigment epitheliums transplantation: Subretinal transplantation of clinical human embryonic stem cell derived retinal pigment epitheliums.
Study summary
This project intends to transplant a clinical level human embryonic stem cells derived retinal pigment epithelium into subretinal space to treat eetinitis pigmentosa(RP) diseases. Through the statistical analysis EDTRS, BCVA, OCT, ERG, Fluorescein angiography, Ophthalmic AB ultrasound changes between before and after the treatment to assess the efficacy and safety 0f RPE transplants to treat RP disease.
Eligibility
Primary outcome measure(s)
- Adverse events and serious adverse events occurred within 1 year after transplantation — one year
The occurrence of adverse events (AE), severe adverse events (SAE), treatment-related adverse events (TEAE), and clinically significant vital signs during the study period.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Beijing Tongren Hospitol,Capital Medical University | Beijing | Beijing Municipality |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT03944239 on ClinicalTrials.gov ↗ ← All trials in China