Your session is about to expire
← Back to Search
Stem Cell Therapy
Stem Cells for Retinal Disease
Phase 1
Waitlist Available
Led By Susanna s Park, MD PhD
Research Sponsored by University of California, Davis
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Age >18 years of age
Vision loss from macular degeneration, retinitis pigmentosa, retinal vein occlusion, or diabetic retinopathy
Must not have
Other concurrent retinal or optic nerve disease affecting vision
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 day to 6 months
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing if injecting special cells from bone marrow into the eye is safe and possible for patients who are permanently blind due to retinal diseases. The hope is that these cells can help fix the damaged parts of their eyes.
Who is the study for?
This trial is for adults over 18 with vision loss from conditions like macular degeneration or diabetic retinopathy. Participants must have a visual acuity ranging from 20/100 to hand movement and the affected eye should be the one with worse vision. They shouldn't have had certain eye treatments in the last 6 months, no blood disorders, active diseases, or be on immunosuppressive therapy.
What is being tested?
The study tests injecting CD34+ stem cells directly into the eye of patients who are blind due to various retinal diseases. It aims to assess if this approach is safe and can feasibly improve sight.
What are the potential side effects?
Potential side effects may include discomfort at injection site, inflammation inside the eye, increased intraocular pressure, bleeding, infection risk post-procedure and possible immune reaction.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am older than 18 years.
Select...
I have vision loss due to a specific eye condition.
Select...
I haven't had treatments for eye swelling or abnormal blood vessels in the eye in the last 6 months.
Select...
I am not on any immunosuppressive therapy.
Select...
I have had vision loss for more than 3 months.
Select...
I do not have any active eye or systemic diseases.
Select...
I do not have any blood clotting or blood disorders.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have an eye condition affecting my vision.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 day to 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 day to 6 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Incidence and severity of ocular adverse events
Secondary study objectives
The number of stem cells isolated and injected into the study eye
Other study objectives
Incidence and severity of systemic adverse events
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Stem cell treatedExperimental Treatment1 Intervention
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for Diabetic Retinopathy include anti-VEGF injections, corticosteroids, laser therapy, and vitrectomy. Anti-VEGF injections work by inhibiting vascular endothelial growth factor, reducing abnormal blood vessel growth and leakage.
Corticosteroids reduce inflammation and edema in the retina. Laser therapy seals leaking blood vessels and prevents further vision loss.
Vitrectomy removes blood and scar tissue from the vitreous. These treatments are crucial as they help manage symptoms and prevent progression of the disease.
Similar to these treatments, the CD34+ stem cell injection trial aims to repair or replace damaged retinal cells, offering a regenerative approach that could potentially restore vision and address the underlying damage caused by Diabetic Retinopathy.
Find a Location
Who is running the clinical trial?
University of California, DavisLead Sponsor
939 Previous Clinical Trials
4,739,734 Total Patients Enrolled
2 Trials studying Retinitis Pigmentosa
442 Patients Enrolled for Retinitis Pigmentosa
Susanna s Park, MD PhDPrincipal InvestigatorUniversity of California Davis Eye Center
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- Your eyes do not have any major blockages or cloudiness.I am older than 18 years.I have vision loss due to a specific eye condition.I haven't had treatments for eye swelling or abnormal blood vessels in the eye in the last 6 months.I am not on any immunosuppressive therapy.I have an eye condition affecting my vision.I do not have any active eye or systemic diseases.I am not on any immunosuppressive therapy.I have vision loss due to a specific eye condition.I am older than 18 years.I have been experiencing vision loss for more than 3 months.I haven't had treatments for eye swelling or abnormal blood vessels in the eye in the last 6 months.I have had vision loss for more than 3 months.I do not have any active eye or systemic diseases.I do not have any blood clotting or blood disorders.My blood's ability to clot is normal.Your eye with the worst vision will be considered for the study.
Research Study Groups:
This trial has the following groups:- Group 1: Stem cell treated
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Share this study with friends
Copy Link
Messenger