Stem Cell Ophthalmology Treatment Study

Glaucoma Clinical Trial

— SCOTS  

Official title:

Bone Marrow Derived Stem Cell Ophthalmology Treatment Study

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

• NCT number: NCT01920867
• Other study ID #: ICMS-2013-0019.
• Status: Enrolling by invitation
• Phase: N/A
• Start date: August 2012
• Est. completion date: July 2020

Study information

• Verified date: October 2019
• Source: MD Stem Cells
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will evaluate the use of autologous bone marrow derived stem cells (BMSC) for the treatment of retinal and optic nerve damage or disease. http://mdstemcells.com/scots-ii/

Description:

Eyes with loss of vision from retinal or optic nerve conditions generally considered irreversible will be treated with a combination of injections of autologous bone marrow derived stem cells isolated from the bone marrow using standard medical and surgical practices. Retinal conditions may include degenerative, ischemic or physical damage ( examples may include macular degeneration, hereditary retinal dystrophies such as retinitis pigmentosa, stargardt, non-perfusion retinopathies, post retinal detachment. Optic Nerve conditions may include degenerative, ischemic or physical damage ( examples may include optic nerve damage from glaucoma, compression, ischemic optic neuropathy, optic atrophy ). Injections may include retrobulbar, subtenon, intravitreal, intraocular, subretinal and intravenous. Patients will be followed for 12 months with serial comprehensive eye examinations including relevant imaging and diagnostic ophthalmic testing.

Recruitment information / eligibility

• Status: Enrolling by invitation
• Enrollment: 300
• Est. completion date: July 2020
• Est. primary completion date: July 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Have objective, documented damage to the retina or optic nerve unlikely to improve OR

• Have objective, documented damage to the retina or optic nerve that is progressive

• AND have less than or equal to 20/40 best corrected central visual acuity in one or both eyes AND/OR an abnormal visual field in one or both eyes.

• Be at least 3 months post-surgical treatment intended to treat any ophthalmologic disease and stable.

• If under current medical therapy ( pharmacologic treatment) for a retinal or optic nerve disease be considered stable on that treatment and unlikely to have visual function improvement ( for example, glaucoma with intraocular pressure stable on topical medications but visual field damage ).

• Have the potential for improvement with BMSC treatment and be at minimal risk of any potential harm from the procedure.

• Be over the age of 18

• Be medically stable and able to be medically cleared by their primary care physician or a licensed primary care practitioner for the procedure. Medical clearance means that in the estimation of the primary care practitioner, the patient can reasonably be expected to undergo the procedure without significant medical risk to health.

Exclusion Criteria:

• Patients who are not capable of an adequate ophthalmologic examination or evaluation to document the pathology.

• Patients who are not capable or not willing to undergo follow up eye exams with the principle investigator or their ophthalmologist or optometrist as outlined in the protocol.

• Patients who are not capable of providing informed consent.

• Patients who may be at significant risk to general health or to the eyes and visual function should they undergo the procedure.

Related Conditions & MeSH terms

• Glaucoma
• Hereditary Retinal Dystrophy
• Macular Degeneration
• Nervous System Diseases
• Optic Nerve Disease
• Optic Nerve Diseases
• Retinal Disease
• Retinal Diseases
• Retinal Dystrophies

Intervention

Procedure:
• RB (Retrobulbar)
Retrobulbar injection of Bone Marrow Derived Stem Cells (BMSC)
• ST (Subtenon)
Subtenon injection of Bone Marrow Derived Stem Cells (BMSC)
• IV (Intravenous)
Intravenous injection of Bone Marrow Derived Stem Cells (BMSC)
• IVIT (Intravitreal)
Intravitreal injection of Bone Marrow Derived Stem Cells (BMSC)
• IO (Intraocular)
Intraocular injection of Bone Marrow Derived Stem Cells (BMSC) with vitrectomy prior to intraocular injection. For example, may include larger amount of stem cells in the intravitreal cavity, intraneuronal injections or subretinal injections of stem cells.

Locations

Country	Name	City	State
United States	MD Stem Cells	Westport	Connecticut

Sponsors (1)

Lead Sponsor	Collaborator
MD Stem Cells

Country where clinical trial is conducted

United States, 

References & Publications (3)

Weiss JN, Benes SC, Levy S. Stem Cell Ophthalmology Treatment Study (SCOTS): improvement in serpiginous choroidopathy following autologous bone marrow derived stem cell treatment. Neural Regen Res. 2016 Sep;11(9):1512-1516. — View Citation

Weiss JN, Levy S, Benes SC. Stem Cell Ophthalmology Treatment Study (SCOTS) for retinal and optic nerve diseases: a case report of improvement in relapsing auto-immune optic neuropathy. Neural Regen Res. 2015 Sep;10(9):1507-15. doi: 10.4103/1673-5374.1655 — View Citation

Weiss JN, Levy S, Malkin A. Stem Cell Ophthalmology Treatment Study (SCOTS) for retinal and optic nerve diseases: a preliminary report. Neural Regen Res. 2015 Jun;10(6):982-8. doi: 10.4103/1673-5374.158365. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Visual acuity	Best corrected visual acuity will be measured with Snellen Eye Chart and the ETDRS (Early Treatment Diabetic Retinopathy Study)Eye Chart when available at each post- procedure visit. Intervals at minimum will be first post- procedure day,then 3 months, 6 months and 12 months post-procedure day. Recommended visit 1 month post -procedure day.	1 day to 12 months
Secondary	Visual fields	Visual fields will be evaluated with automated perimetry during post- procedure visits as needed and specifically at 6 months and 12 months.	1 day to 12 months

External Links

•   The Role of Patient Funded Clinical Research in Advancing Medical Care