Autologous Bone Marrow-Derived Stem Cells Transplantation For Retinitis Pigmentosa (RETICELL)
Primary Purpose
Retinitis Pigmentosa
Status
Completed
Phase
Phase 2
Locations
Brazil
Study Type
Interventional
Intervention
intravitreal injection of autologous bone marrow stem cells
Sponsored by
About this trial
This is an interventional treatment trial for Retinitis Pigmentosa focused on measuring Retinitis pigmentosa, stem cell, bone marrow, retinal dysprophy
Eligibility Criteria
Inclusion Criteria:
- diagnosis of retinitis pigmentosa logarithm of minimum angle of resolution (logMAR) BCVA of 1.0 (Snellen equivalent, 20/200) or worse
- visual Field less than 20 degreees
Exclusion Criteria:
- previous ocular surgery other than cataract
- presence of cataract or other media opacity that would influence ocular fundus documentation and adequate ERG and visual field evaluation
- other ophthalmic disease like glaucoma and uveitis
- previous history of blood disorders like leukemia
- known allergy to fluorescein or indocyanine green
- known coagulation abnormalities or current use of anticoagulative medication other than aspirin.
Sites / Locations
- Centro de Pesquisa Rubens Siqueira
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Experimental: Test group
Arm Description
Retinitis pigmentosa patients with best-corrected visual acuity (BCVA) worse than 20/200 or visual field less than 20 degrees
Outcomes
Primary Outcome Measures
ETDRS Visual acuity change
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01560715
Brief Title
Autologous Bone Marrow-Derived Stem Cells Transplantation For Retinitis Pigmentosa
Acronym
RETICELL
Official Title
Phase 2 Study Of Autologous Bone Marrow-Derived Stem Cells Transplantation For Retinitis Pigmentosa
Study Type
Interventional
2. Study Status
Record Verification Date
July 2017
Overall Recruitment Status
Completed
Study Start Date
June 2011 (undefined)
Primary Completion Date
January 2013 (Actual)
Study Completion Date
June 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Sao Paulo
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to evaluate the short-term safety and efficacy of a single intravitreal injection of autologous bone marrow stem cells in patients with retinitis pigmentosa.
Detailed Description
A prospective phase II, nonrandomized open-label study of retinitis pigmentosa patients with best-corrected ETDRS visual acuity (BCVA) worse than 20/200. Standardized ophthalmic evaluation will be perform at baseline and at weeks 1, 4,12 and 24 (±1) following intravitreal injection of 10 x 106 bone marrow stem cells/ 0,1ml . Three measures will be used to evaluate the short-term safety of intravitreal of ABMDSC: 1) severe visual loss, defined as a drop in 15 letters on ETDRS visual acuity scale; 2) decrease in ERG response; 3) decrease in 5 square degrees on visual field; secondary safety outcomes : 1) increase in intra-ocular inflammation defined herein as anterior chamber cells and flare higher than 3+ for more than 1 month after injection according to a classification described elsewhere ; 2) decrease in CMT more than 50um; 3)genesis of abnormal tissues (teratomas) or tumors; 4) qualitative changes in retinal or choroidal perfusion, like macular nonperfusion. Secondary outcome measures will be used to evaluate the short-term efficiency of intravitreal of ABMDSC: 1) improvement in ERG response; 2) increase in visual field: 3) increase in CSMT > 50um and not related to macular edema; 4) increase > 5 letters on BCVA
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Retinitis Pigmentosa
Keywords
Retinitis pigmentosa, stem cell, bone marrow, retinal dysprophy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Experimental: Test group
Arm Type
Experimental
Arm Description
Retinitis pigmentosa patients with best-corrected visual acuity (BCVA) worse than 20/200 or visual field less than 20 degrees
Intervention Type
Biological
Intervention Name(s)
intravitreal injection of autologous bone marrow stem cells
Other Intervention Name(s)
autologous bone marrow stem cells
Intervention Description
One intravitreal injection of a 0.1-ml cell suspension containing around 10x106 bone marrow mononuclear stem cells(BMMSC). All treatments were performed by a single retinal specialist using topical proparacaine drops under sterile conditions (eyelid speculum and povidone-iodine). Autologous BMMSC were injected into the vitreous cavity using a 27 gauge needle inserted through the inferotemporal pars plana 3.0 - 3.5 mm posterior to the limbus. After the injection, central retinal artery perfusion was confirmed with indirect ophthalmoscopy. Patients were instructed to instill one drop of 0.3% ciprofloxacin into the injected eye four times daily for 1 week after the procedure.
Primary Outcome Measure Information:
Title
ETDRS Visual acuity change
Time Frame
Day 1 to Day 365
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
diagnosis of retinitis pigmentosa logarithm of minimum angle of resolution (logMAR) BCVA of 1.0 (Snellen equivalent, 20/200) or worse
visual Field less than 20 degreees
Exclusion Criteria:
previous ocular surgery other than cataract
presence of cataract or other media opacity that would influence ocular fundus documentation and adequate ERG and visual field evaluation
other ophthalmic disease like glaucoma and uveitis
previous history of blood disorders like leukemia
known allergy to fluorescein or indocyanine green
known coagulation abnormalities or current use of anticoagulative medication other than aspirin.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rubens C Siqueira, MD,PhD
Organizational Affiliation
Sao Paulo University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centro de Pesquisa Rubens Siqueira
City
Sao Jose do Rio Preto
State/Province
SP
ZIP/Postal Code
15010-100
Country
Brazil
12. IPD Sharing Statement
Citations:
PubMed Identifier
21293313
Citation
Siqueira RC, Messias A, Voltarelli JC, Scott IU, Jorge R. Intravitreal injection of autologous bone marrow-derived mononuclear cells for hereditary retinal dystrophy: a phase I trial. Retina. 2011 Jun;31(6):1207-14. doi: 10.1097/IAE.0b013e3181f9c242.
Results Reference
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PubMed Identifier
25890251
Citation
Siqueira RC, Messias A, Messias K, Arcieri RS, Ruiz MA, Souza NF, Martins LC, Jorge R. Quality of life in patients with retinitis pigmentosa submitted to intravitreal use of bone marrow-derived stem cells (Reticell -clinical trial). Stem Cell Res Ther. 2015 Mar 14;6(1):29. doi: 10.1186/s13287-015-0020-6.
Results Reference
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PubMed Identifier
23049424
Citation
Siqueira RC. Stem cell therapy in retinal diseases? Rev Bras Hematol Hemoter. 2012;34(3):222-6. doi: 10.5581/1516-8484.20120054. No abstract available.
Results Reference
background
PubMed Identifier
23000646
Citation
Siqueira RC, Messias A, Voltarelli JC, Messias K, Arcieri RS, Jorge R. Resolution of macular oedema associated with retinitis pigmentosa after intravitreal use of autologous BM-derived hematopoietic stem cell transplantation. Bone Marrow Transplant. 2013 Apr;48(4):612-3. doi: 10.1038/bmt.2012.185. Epub 2012 Sep 24. No abstract available.
Results Reference
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Autologous Bone Marrow-Derived Stem Cells Transplantation For Retinitis Pigmentosa
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