CB-PRP in Retinitis Pigmentosa and Dry Age-related Macular Degeneration (SiCord)
Primary Purpose
Retinitis Pigmentosa, Dry Age-related Macular Degeneration
Status
Completed
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
Subretinal injection of umbilical cord blood platelet-rich plasma (CB-PRP)
Sponsored by
About this trial
This is an interventional treatment trial for Retinitis Pigmentosa focused on measuring Cord blood platelet-rich plasma, Retinitis pigmentosa, Dry Age-related Macular degeneration, Macular Geographic Atrophy
Eligibility Criteria
Inclusion Criteria:
- Retinal dystrophies with compromised rods (only for RP patients)
- Visual Field (Manual Goldmann) V / 4e < 30 ° (only for RP patients)
- Best corrected visual acuity > Light perception
- Known genotype
- No or minimal opacity of ocular media
- No concomitant ocular (eg glaucoma, amblyopia)
- Dry Age-related Macular Degeneration (Geographic type)
Exclusion Criteria:
- Age<18 years
- Pregnancy
- Previous inflammatory / infectious events involving the eyes
Sites / Locations
- Alfonso Savastano
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Affected Individual
Arm Description
A subretinal injection of umbilical cord blood platelet-rich plasma (CB-PRP) will be performed only in one eye, the other eye will be considered as a control group.
Outcomes
Primary Outcome Measures
Optical coherence tomography (OCT) and optical coherence tomography angiography (OCTA) morphological changes
Differences in structural optical coherence tomography (OCT) and OCT Angiography (OCTA) images
Secondary Outcome Measures
Full Information
NCT ID
NCT04636853
First Posted
November 14, 2020
Last Updated
January 9, 2023
Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
1. Study Identification
Unique Protocol Identification Number
NCT04636853
Brief Title
CB-PRP in Retinitis Pigmentosa and Dry Age-related Macular Degeneration
Acronym
SiCord
Official Title
Cord Blood Platelet-rich Plasma (CB-PRP) in Retinitis Pigmentosa and Dry Age-related Macular Degeneration
Study Type
Interventional
2. Study Status
Record Verification Date
December 2020
Overall Recruitment Status
Completed
Study Start Date
December 23, 2020 (Actual)
Primary Completion Date
December 1, 2021 (Actual)
Study Completion Date
December 2, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The study will provides the enrollment of patients with genetic retinal dystrophies with primary rod impairment and dry age-related macular degeneration (Geographic type) A subretinal injection of umbilical cord blood platelet-rich plasma (CB-PRP) will be performed only in one eye, the other eye will be considered as a control group.
A complete morpho-functional ophthalmological evaluation will be performed in all patients at each control.
Detailed Description
All patients underwent genetic evaluation and they reported different types of mutations that induce anatomic-functional impairment of the rods.
Patients affected by bilateral dry age-related macular degeneration (Geographic type) will be recruited as well.
After selecting the patients to be enrolled, the study will proceed with the vitrectomy surgery and subretinal injection of umbilical cord blood platelet-rich plasma (CB-PRP) provided by the Umbilical Cord Bank according to the procedures provided for by the current legislation on blood components for non-transfusion use.
A complete ophthalmological examination will be performed at 1, 3, 6, and 12 months. They will include:
Anterior segment biomicroscopy
direct and indirect ophthalmoscopy
ETDRS visual acuity assessment
intraocular pressure measurement
optical coherence tomography (OCT)
OCT Angiography (OCTA)
The following assessments will be performed at baseline and at 6 and 12 months.
Microperimetry
Electroretinogram (ERG)
Visually evoked potential (VEP)
contrast sensitivity (MARS tables)
Goldmann perimetry
Some morpho-functional data will also be collected in the contralateral eye and used as the control group.
To ensure the best safety for the patient, the first 5 eyes will be separated by a minimum of 20 days in order to observe the post-surgical evolution.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Retinitis Pigmentosa, Dry Age-related Macular Degeneration
Keywords
Cord blood platelet-rich plasma, Retinitis pigmentosa, Dry Age-related Macular degeneration, Macular Geographic Atrophy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Sequential Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Affected Individual
Arm Type
Experimental
Arm Description
A subretinal injection of umbilical cord blood platelet-rich plasma (CB-PRP) will be performed only in one eye, the other eye will be considered as a control group.
Intervention Type
Biological
Intervention Name(s)
Subretinal injection of umbilical cord blood platelet-rich plasma (CB-PRP)
Intervention Description
A subretinal injection of umbilical cord blood platelet-rich plasma (CB-PRP) will be performed only in one eye, the other eye will be considered as a control group.
A complete morpho-functional ophthalmological evaluation will be performed in all patient at each control.
Primary Outcome Measure Information:
Title
Optical coherence tomography (OCT) and optical coherence tomography angiography (OCTA) morphological changes
Description
Differences in structural optical coherence tomography (OCT) and OCT Angiography (OCTA) images
Time Frame
3 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Retinal dystrophies with compromised rods (only for RP patients)
Visual Field (Manual Goldmann) V / 4e < 30 ° (only for RP patients)
Best corrected visual acuity > Light perception
Known genotype
No or minimal opacity of ocular media
No concomitant ocular (eg glaucoma, amblyopia)
Dry Age-related Macular Degeneration (Geographic type)
Exclusion Criteria:
Age<18 years
Pregnancy
Previous inflammatory / infectious events involving the eyes
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alfonso Savastano
Organizational Affiliation
Fondazione Policlinico Universitario A. Gemelli, IRCCS
Official's Role
Principal Investigator
Facility Information:
Facility Name
Alfonso Savastano
City
Rome
ZIP/Postal Code
00168
Country
Italy
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
30858959
Citation
Valentini CG, Nuzzolo ER, Bianchi M, Orlando N, Iachininoto MG, Pinci P, Teofili L. Cord Blood Platelet Lysate: In Vitro Evaluation to Support the Use in Regenerative Medicine. Mediterr J Hematol Infect Dis. 2019 Jan 1;11(1):e2019021. doi: 10.4084/MJHID.2019.021. eCollection 2019.
Results Reference
result
Learn more about this trial
CB-PRP in Retinitis Pigmentosa and Dry Age-related Macular Degeneration
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