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The preliminary clinical study of bone marrow mesenchymal stem cells infusion treatment of retinitis pigmentosa

The preliminary clinical study of bone marrow mesenchymal stem cells infusion treatment of retinitis pigmentosa

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TNRC-14004694
Enrollment
Unknown
Registered
2014-05-21
Start date
2014-01-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

retinitis pigmentosa

Interventions

case series:autologous bone marrow mesenchymal stem cell infusion therapy

Sponsors

Southwest Hospital, Third Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patient has signed informed consent for retinal transplantation and is willing to return for follow-up visits;2. Age range 18 to 65 years,gender unlimited; 3.Patients with at least one eye (monocular) or both eyes suffering from impaired vision caused by retinitis pigmentosa; 4.Use the early treatment diabetic retinopathy (ETDRs) eye chart in 4 meters distance detection, best corrected visual acuity scores between 19 and 73 letter, including 19 and 73 (or the equivalent of about Snellen eyesight from 20/400 to 20/40).

Exclusion criteria

Exclusion criteria: 1. Patient has medical problems that have a high risk of general anesthesia, such as metabolic, cadiovascular, hematopoietic or psychological system disorders; 2. Women in menstruation, pregnancy, perinatal prtiod and baby nursing periods; 3. Any significant ocular disease that has compromised or could compromise vision in the study eye and confound analysis of the primary outcome; 4. Patient who has a history of corneal leukoma, cataract, uveitis, Coat’s disease, diabetic retinopathy, glaucoma, or vitreous opacities that prevents visualization of the posterior pole; 5. Participating in another ophthalmic clinical trial or use of any other investigational new drugs within 3 months before the start of study treatment; 6. Intraocular surgery within the last 3 months.

Design outcomes

Primary

MeasureTime frame
Early treatment of diabetic retinopathy eye chart(;Fluorescein angiography;Static perimetry;Optical coherent tomography(OCT);Flash electroretinogram(FERG);Flash Visual Evoked Potentials(FVEP);mutifocal electroretinogram(MFERG);Pupillary light refle;

Countries

China

Contacts

Public ContactYin Zhengqin
qinzyin@aliyun.com+86 023 68754401

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026