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ACTIVE NOT RECRUITING Phase 1

Clinical Trial of Autologous Intravitreal Bone-marrow CD34+ Stem Cells for Retinopathy

NCT01736059 · View on ClinicalTrials.gov ↗

Study Summary

This pilot study is to determine whether it would be safe and feasible to inject CD34+ stem cells from bone marrow into the eye as treatment for patients who are irreversibly blind from various retinal conditions.

Interventions

  • DRUG CD34+ bone marrow stem cells intravitreal

Study Locations (1)

California

  • University of California Davis — Sacramento

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2012-07
Est. Completion 2026-10
Phase Phase 1

Sponsor

University of California, Davis

653 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01736059

The ClinicalTrials.gov registry entry for NCT01736059 describes a study currently listed as active not recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, Davis, which has 653 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 5 conditions, with Diabetic Retinopathy appearing as the primary indexed condition, and to 1 intervention — of which CD34+ bone marrow stem cells intravitreal is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01736059 reports 1 study location spanning 1 distinct geographic area — top geographies include California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT01736059 about?

NCT01736059 is a clinical study titled "Clinical Trial of Autologous Intravitreal Bone-marrow CD34+ Stem Cells for Retinopathy". This pilot study is to determine whether it would be safe and feasible to inject CD34+ stem cells from bone marrow into the eye as treatment for patients who are irreversibly blind from various retinal conditions.

What is the current status of trial NCT01736059?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 15 participants. The study started on 2012-07. Estimated completion is 2026-10.

What conditions does trial NCT01736059 study?

This clinical trial studies the following conditions: Diabetic Retinopathy, Retinitis Pigmentosa, Non-exudative Age-related Macular Degeneration, Retina Vein Occlusion, Hereditary Macular Degeneration. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01736059?

The interventions under investigation include: CD34+ bone marrow stem cells intravitreal (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01736059?

This trial is sponsored by University of California, Davis, which has 653 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01736059 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial