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The Effect of Stem Cells and Stem Cell Exosomes on Visual Functions in Patients With Retinitis Pigmentosa

Primary Purpose

Retinitis Pigmentosa

Status
Recruiting
Phase
Phase 2
Locations
Turkey
Study Type
Interventional
Intervention
Subtenon injection of Wharton jelly derived mesenchymal stem cells
Subtenon injection of Wharton jelly derived mesenchymal stem cell exosomes
Placebo
Sponsored by
TC Erciyes University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Retinitis Pigmentosa focused on measuring wharton jelly derived, mesenchymal stem cell, exosome

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 18 years and over,
  • Diagnosis of retinitis pigmentosa: by clinical history, fundus examination, visual field (GA), electroretinogram (ERG), and genetic analysis
  • Visual field loss
  • The best corrected visual acuity of 0.05 on the Snellen chart
  • The MD (mean deviation) value in the visual field is between 33.0 and -5.0 dB
  • Intraocular pressure value below 22 mmHg

Exclusion Criteria:

  • Presence of cataracts or other media opacities that may affect imaging and tests
  • Diagnosis of glaucoma
  • History of ocular surgery or injection in the last 6 months
  • Visual level too low for examinations (0.05 and below)
  • Diagnosis of any systemic disease (such as diabetes, uncontrolled hypertension, neurological disease)
  • Smoking and substance abuse

Sites / Locations

  • Erciyes University, Faculty of MedicineRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

Wharton jelly-derived mesenchymal stem cell

Mesenchymal stem cell exosome (Wharton jelly-derived)

Placebo

Arm Description

Single subtenon injection of Wharton jelly-derived mesenchymal stem cells will be performed on a single eye after randomization

Single subtenon injection of mesenchymal stem cell exosomes (Wharton jelly-derived)will be performed on a single eye after randomization.

A single subtenon injection of saline will be performed on a single eye after randomization.

Outcomes

Primary Outcome Measures

Evaluation of best corrected visual acuity change
Visual acuity change with LogMar Chart
Evaluation of visual field change
Mean deviation values of automatic visual field testing

Secondary Outcome Measures

Evaluation of multifocal ERG changes
Amplitudes changes in multifocal ERG testing
Evaluation of ERG changes
Amplitude changes in multifocal ERG testing
Evaluation of optical coherence tomography changes
Retinal thickness changes in optical coherence tomography change
Evaluation of optical coherence tomography angiography changes
Vascular density changes in optical coherence tomography angiography

Full Information

First Posted
May 28, 2022
Last Updated
September 5, 2022
Sponsor
TC Erciyes University
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1. Study Identification

Unique Protocol Identification Number
NCT05413148
Brief Title
The Effect of Stem Cells and Stem Cell Exosomes on Visual Functions in Patients With Retinitis Pigmentosa
Official Title
The Effect of Wharton Jelly-derived Mesenchymal Stem Cells and Stem Cell Exosomes on Visual Functions in Patients With Retinitis Pigmentosa
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Recruiting
Study Start Date
August 5, 2022 (Actual)
Primary Completion Date
July 1, 2023 (Anticipated)
Study Completion Date
December 15, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
TC Erciyes University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This clinical trial aims to study the efficacy of umbilical cord-derived mesenchymal stem cells and their exosomes in the treatment of retinitis pigmentosa. The participants will be randomized into 3 groups. Functional and structural parameters will be compared before and after the injections and also will be compared among the groups to reveal whether stem cell and their exosomes are more effective than placebo.
Detailed Description
Retinitis pigmentosa (RP) is one of the leading causes of vision loss and irreversible blindness. It is stated that 1.4 million people are affected in the world and its prevalence is 1:4000. Stem cell applications are methods that are increasingly gaining importance in the field of regenerative medicine and ophthalmology. In addition to many experimental studies in retinal diseases including retinitis pigmentosa, there are also clinical studies reporting successful results on humans. The most widely used stem-cell group in current clinical practice is mesenchymal stem cells. The advantages are that they are relatively easy to obtain and do not induce severe immune responses. Clinical studies in stem cell therapies for the eye suggest that stem cells benefit the surrounding tissue by secreting support such as growth factors, and extracellular vesicles, mostly due to their trophic and paracrine effects. In intraocular applications, there has been a tendency to apply mesenchymal stem cells around/outside the eye, including subtenon and suprachoroidal application due to side effects such as retinal detachment and epiretinal membrane. Other cellular products that have been studied in animal studies and clinical research in recent years are exosomes. Exosomes are a subgroup of extracellular vesicles released from cells. Exosomes are extracellular vesicles 30-150 nm in size and carry at least one of the exosomal proteins CD63, CD9, CD81, syntenin-1 and TSG101. Exosomes are secreted from different cells in the organism and are also found in body fluids. Exosomes play a role in the transportation of biomolecules such as lipids, carbohydrates, nucleic acids and proteins from one cell to another and in this way, they function in genetic information transfer, and reprogramming of the opposite cell and intercellular communication. One of the sources of exosomes is mesenchymal stem cells that secrete high amount of exosomes. Mesenchymal stem cell-derived exosomes have been reported to have therapeutic effects, just like mesenchymal stem cells. It is thought that stem cells also exert their clinical effects through paracrine factors they secrete rather than being implanted in the tissue. However, the mechanism of action of mesenchymal stem cells has not been fully understood, and exosomes are thought to contribute to the effect. The storage and durability of exosomes may provide advantages in therapeutic applications compared to mesenchymal stem cells and may provide more immunological advantages in allogeneic applications compared to cellular treatments since they do not contain cells. One of the sources from which mesenchymal stem cells can be obtained is Wharton jelly, which is the mesenchymal tissue of the umbilical cord. Stem cells originating from Wharton gel are a good source of stem cells due to their high differentiation capacity, high regeneration capacity, constant doubling time, high proliferation capacity, low immunogenicity, and no ethical problems due to non-invasive methods, and easy availability. This clinical trial will enroll patients diagnosed with retinitis pigmentosa. The diagnosis of RP is made by clinical fundus examination, examinations in our clinic, and genetic analysis. At the beginning of the study, all volunteers will undergo a full ophthalmologic examination including best-corrected visual acuity, anterior segment and fundus examination with a slit lamp, OCT (optical coherence tomography), VF (visual field), ERG (electroretinogram), mfERG (multifocal ERG), OCTA (optical coherence tomography). Retinal and choroidal thickness and ellipsoid bandwidth in OCT, MD (mean deviation) value showing sensitivity in VF, amplitude and latency times in ERG and mf-ERG, vascular density and vascular flow ratios in OCTA will be recorded. The volunteers will be randomized into three. The 1st group will be the placebo group (45 volunteers) and 0.5 cc saline physiological saline will be applied to the subtenon space. 2nd group of patients (45 volunteers) will undergo a subtenon injection of Wharton gel-derived mesenchymal stem cell suspension. A suspension containing mesenchymal stem cell exosomes from Wharton jelly will be applied to the subtenon distance to the 3rd group of patients (45 volunteers). A single eye of each volunteer will be included. Informed consent will be obtained from the volunteers. Allogeneic human Wharton gel tissue-derived mesenchymal stem cells and their exosomes will be obtained from healthy female volunteers, who is over 18 years old, under sterile conditions after HBV, HCV, HIV virus and "Treponema Pallidum" (VDRL) tests were performed. Cord tissue obtained from birth will be carried in a sterile transfer solution and will be processed to obtain stem cells in Erciyes University Genome and Stem Cell GMP (good manufacturing practices) certified laboratories. Exosomes will be obtained by the ultracentrifugation method in the same facility. For injection into the subtenon distance, the conjunctiva and tenon will be opened with a small incision about 10 mm away from the lower temporal area, then 20 gauge curved subtenon cannula will be advanced parallel to the sclera and injected into the posterior subtenon area. All volunteers will be prescribed antibiotics and steroid drops after the surgical procedure. Full ophthalmological examination and examinations at the beginning of the study will be performed and recorded again on the 1st day, 1st month, 2nd month, 3rd month and 6th months of the anterior segment and fundus examination, OCT (optical coherence tomography), VF (visual field) ), ERG (electroretinogram), mfERG (multifocal ERG), OCTA (optical coherence tomography) examinations will be performed. In addition, a questionnaire evaluating the visual functions subjectively will be administered at the 1st, 3rd and 6th-month visits. (National Eye Institute Visual Functioning Questionnaire - 25 / National Eye Institute (USA) Visual Function Questionnaire ). Two masked investigators will perform analyses. Post-procedure 1st Day, 1st Month, 2nd Month, 3rd Month and 6th Month data will be compared among study groups and within groups.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Retinitis Pigmentosa
Keywords
wharton jelly derived, mesenchymal stem cell, exosome

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
135 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Wharton jelly-derived mesenchymal stem cell
Arm Type
Active Comparator
Arm Description
Single subtenon injection of Wharton jelly-derived mesenchymal stem cells will be performed on a single eye after randomization
Arm Title
Mesenchymal stem cell exosome (Wharton jelly-derived)
Arm Type
Active Comparator
Arm Description
Single subtenon injection of mesenchymal stem cell exosomes (Wharton jelly-derived)will be performed on a single eye after randomization.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
A single subtenon injection of saline will be performed on a single eye after randomization.
Intervention Type
Biological
Intervention Name(s)
Subtenon injection of Wharton jelly derived mesenchymal stem cells
Intervention Description
Single subtenon's injection for single eye
Intervention Type
Biological
Intervention Name(s)
Subtenon injection of Wharton jelly derived mesenchymal stem cell exosomes
Intervention Description
Single subtenon's injection for single eye
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Single Subtenon injection of saline for a single eye
Primary Outcome Measure Information:
Title
Evaluation of best corrected visual acuity change
Description
Visual acuity change with LogMar Chart
Time Frame
Upto 6 months
Title
Evaluation of visual field change
Description
Mean deviation values of automatic visual field testing
Time Frame
Upto 6 months
Secondary Outcome Measure Information:
Title
Evaluation of multifocal ERG changes
Description
Amplitudes changes in multifocal ERG testing
Time Frame
Upto 6 months
Title
Evaluation of ERG changes
Description
Amplitude changes in multifocal ERG testing
Time Frame
Upto 6 months
Title
Evaluation of optical coherence tomography changes
Description
Retinal thickness changes in optical coherence tomography change
Time Frame
Upto 6 months
Title
Evaluation of optical coherence tomography angiography changes
Description
Vascular density changes in optical coherence tomography angiography
Time Frame
Upto 6 months

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: 18 years and over, Diagnosis of retinitis pigmentosa: by clinical history, fundus examination, visual field (GA), electroretinogram (ERG), and genetic analysis Visual field loss The best corrected visual acuity of 0.05 on the Snellen chart The MD (mean deviation) value in the visual field is between 33.0 and -5.0 dB Intraocular pressure value below 22 mmHg Exclusion Criteria: Presence of cataracts or other media opacities that may affect imaging and tests Diagnosis of glaucoma History of ocular surgery or injection in the last 6 months Visual level too low for examinations (0.05 and below) Diagnosis of any systemic disease (such as diabetes, uncontrolled hypertension, neurological disease) Smoking and substance abuse
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Osman Ahmet POLAT, MD
Phone
905424395196
Email
osmanahmet@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kuddusi ERKILIÇ, Professor
Organizational Affiliation
Erciyes University Medical Faculty
Official's Role
Principal Investigator
Facility Information:
Facility Name
Erciyes University, Faculty of Medicine
City
Kayseri
ZIP/Postal Code
38039
Country
Turkey
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
OSMAN AHMET POLAT, MD
Phone
+905424395196
Email
osmanpolat@erciyes.edu.tr

12. IPD Sharing Statement

Plan to Share IPD
No
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The Effect of Stem Cells and Stem Cell Exosomes on Visual Functions in Patients With Retinitis Pigmentosa

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