The purpose of this experimental therapy is to evaluate the safety and efficacy of transplantation of autologous olfactory ensheathing cells (OECs) and olfactory nerve fibroblasts (ONFs) obtained from the olfactory bulb with simultaneous reconstruction of the posttraumatic spinal cord gap with peripheral nerve grafts, in patients with chronic complete spinal cord injury. The treatment will be performed in two patients that have sustained an anatomically complete spinal cord transection between the spinal cord segments C5 and Th10. All patients wanting to participate in this study have to send their application at the address: walk-again-project.org
The "Wrocław Walk Again" project is a continuation of the innovative experimental therapy involving reconstruction of patient's severed spinal cords, using their own olfactory glial cells from the olfactory bulb as well as implants from peripheral nerves. The first operation of its kind was performed in 2012. The reconstruction of the cord was a success: the patient regained partial feeling and volitional mobility in paralysed limbs (Cell Transplantation, Vol. 23, pp. 1631-1655, 2014). The experiment's success provided inspiration to continue with the project in order to assess the safety and effectiveness of the therapy applied. The continuation involves planning to qualify two patients with traumatic spinal cord injury, who will then be given treatment and physiotherapy. The programme will be conducted in Wroclaw, Poland, by an interdisciplinary team of doctors and scientists. The Nicholls Spinal Injury Foundation (UK) will be making a significant contribution to the project. Due to this, participants will not need to pay for their experimental treatment or physiotherapy. The main goal of the study is to answer the question if there is possible to evoke functional regeneration of severed spinal cord axons after a two-stage surgical intervention in patients sustaining a complete spinal cord transection between the spinal cord segments C5 and Th10. Patients with clinically, electrophysiologically and radiologically features of complete spinal cord injury will undergo an 8-month neurorehabilitation regimen. Patients who will not show electrophysiological and clinical signs of recovery from the spinal cord injury will enter the surgical part of the study. During the first surgery the patient's own olfactory bulb will be obtained. The human autologous olfactory ensheathing glia and olfactory fibroblast isolated from the olfactory bulb will be used for production of Glial Neuropatch in accordance with the methodology adjusted in grant number GR-797/NCN/2013 and 2012/06/M/NZ4/00138, in a laboratory facility, in accordance with the good manufacture procedures (GMP). The final Product will consist of the aforementioned cell suspension embedded with collagen scaffold. The European Medicines Agency/Committee for Advanced Therapies (EMA/CAT) considers that the Product Glial Neuropatch falls within the definition of a tissue engineered product of an advanced therapy medicinal product (decision EMA/CAT/293903/2018 from 22 June 2018: Scientific recommendation on classification of advanced therapy medicinal products Article 17 - Regulation (EC) No 1394/2007). The second surgery will consist of laminectomy/laminotomy, midline durotomy above the area of spinal cord lesion, detethering of the spinal cord from fibrous adhesions, resection of the posttraumatic spinal cord glial scar, delivering of cultured OEC/ONFs explants (Glial Neuropatch) to the area of spinal cord injury and finally bridging of the spinal cord gap by harvested autologous sural nerve grafts. After discharge from the hospital, the patients will be subjected to a minimum 2-year neurorehabilitation in accordance with the same program as before the operation.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
2
The operative procedure will be aimed to obtain one of the patient's olfactory bulbs. The operation will be performed using a minimally invasive intracranial microsurgical endoscopy-assisted or transnasal endoscopic approach. During the same operation the patient sural nerve will be prepared for a future grafting.
The human autologous olfactory ensheathing glia and olfactory fibroblast isolated from the olfactory bulb will be used for production of Glial Neuropatch in a laboratory facility in accordance with good manufacture procedures (GMP). The final Product will consist of the aforementioned cell suspension embedded with collagen scaffold. The European Medicines Agency/Committee for Advanced Therapies (EMA/CAT) considers that the Product Glial Neuropatch falls within the definition of a tissue engineered product of an advanced therapy medicinal product (decision EMA/CAT/293903/2018 from 22 June 2018: Scientific recommendation on classification of advanced therapy medicinal products Article 17 - Regulation (EC) No 1394/2007).
The surgery will consists of laminectomy/laminotomy, midline durotomy above the area of spinal cord lesion, detethering of the spinal cord from fibrotic adhesions, resection of the posttraumatic spinal cord glial scar, delivering of cultured OEC/ONFs explants (Glial Neuropatch) to the area of spinal cord injury and finally bridging of the spinal cord gap by harvested autologous sural nerve grafts.
Wroclaw Medical University
Wroclaw, Poland
RECRUITINGimprovement of the neurologic state measured by the American Spinal Injury Association (ASIA) score.
A positive outcome will be defined as any detectable improvement of motor and /or sensory function below the level of spinal cord injury, that will result that the patient will change from being with complete spinal cord injury (assigned as ASIA A) to incomplete (ASIA B,C,D or E). ASIA E means complete recovery from spinal cord injury-no clinical evidence of neurological impairment.
Time frame: up to 2 years postoperatively
improvement of the strenght of trunk muscles measured by the Berg Balance scale
a set of tests evaluating the risk of patient to fall during sitting, standing and transfers The results from the specific tests assign the patients to the following three groups: 41-56 points = low fall risk; 21-40 pts. = medium fall risk, 0 -20 pts. = high fall risk An improvement of the trunk muscle strenght that will transfer the patient from the high fall risk group to the medium or low fall risk group will be considered as essential clinical improvement.
Time frame: up to 2 years postoperatively
improvement of neurologic state measured with tests of deep sensation
deep pressure tests applied to the specific dermatomal areas,0 points means no deep sensation while 1 point means sensation of same feeling when pressure is applied
Time frame: up to 2 years postoperatively
improvement of neurologic state measured with tests of vibration
vibration tests applied on the shoulder, elbow, wrist,finger,knee,malleolus and toe 0 Zero, A Diminished, B More vague description - less accurate than A, C Causalgia, 2 Normal
Time frame: up to 2 years postoperatively
improvement of neurologic state measured with tests of joint position sense
joint position test applied on the wrist, thumb, little finger, knee, ankle and great toe 0 points- absence of joint position sense (during 8 of 10 or more attempts) 1. point- impaired sense (correct only on large movements of the joint during 8 of 10 attempts, and incorrect on small movements of the joint (8 of 10 or more attempts) 2. points- normal sense (during 8 of 10 or more attempts) on small and large movements;
Time frame: up to 2 years postoperatively
decrease of muscle spasticity for at least 1 level measured the Ashworth scale
The 5 level spasticity Ashworth scale includes: level 0- no increase in muscle tone, level 1- slight increase in muscle tone, manifested by a catch and release or by minimal, resistance at the end of the range of movement (ROM) when the affected part(s) is moved in flexion or extension, level 2-slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the reminder (less than half) of the ROM, level 3-more marked increase in muscle tone throughout most of the ROM but affected part(s) easily moved, level 4-considerable increase in muscle tone passive, movement difficult, level 5-affected part(s) rigid in flexion or extension
Time frame: tested monthly for at least 2 years postoperatively
Spinal Cord Assessment Tool for Spastic Reflexes ( SCATS)
a test evaluating the clonus rate, and the rate of flexors and extensor muscle spasms Clonus is rated on a 4 point scale that ranges from: 0 No reaction 1. Mild lasting \<3sec 2. Moderate lasting 3-10 seconds 3. Severe lasting \> 10 seconds Flexor spasms are rated on a 4 point scale that ranges from: 0 No reaction 1. Mild, less than 10 degrees of excursion in flexion at knee and hip, or extension of the great toe 2. Moderate = 10-30 degrees of flexion at knee and hip 3. Severe with \>30 degrees of hip and knee flexion SCATS extensor spasms assessment 0 No reaction 1. Mild lasting \<3sec 2. Moderate lasting 3-10 seconds 3. Severe lasting \> 10 seconds Test interpretation: The better the patient improvement is, the lower points he will be assigned, reaching at the end the ideal state of being without clonus and muscle spasms (0 points).
Time frame: tested monthly for at least 2 years postoperatively
improvement of locomotion ability in the Walking Index for Spinal Cord Injury (WISCI II) test,
The WISCI II test assesses the patient walking ability from being unable to walk (0 level) to being able to walk normally without any help (level 20). Interpretation of the test: Any patient improvement that will assign him to a higher level of walking independency compared to the preoperative state will be considered as positive outcome.
Time frame: tested monthly for at least 2 years postoperatively
10 meter walking test
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
a test measuring the velocity of walking the distance of 10 meters; (only the middle 6 meters are timed); Any improvement of the ambulation velocity will be considered as positive outcome.
Time frame: tested monthly for at least 2 years postoperatively
2 minutes walking test
a test measuring the distance ambulated in 2 minutes \[m\] Any improvement of the distance of ambulation in the period of 2 minutes will be considered as positive outcome.
Time frame: tested monthly for at least 2 years postoperatively
time up and go test
The patient should sit on a standard arm chair, placing his/her back against the chair and resting his/her arms chair's arms. Any assistive device used for walking should be nearby. Regular footwear and customary walking aids should be used. The patient should walk to a line that is 3 meters (9.8 feet) away, turn around at the line, walk back to the chair, and sit down. Any decrease of the time needed for completion of this test will be considered as positive outcome.
Time frame: tested monthly for at least 2 years postoperatively
improvement measured by the spinal cord independence measure (SCIM III) test
improvement of the patient self care ability
Time frame: tested monthly for at least 2 years postoperatively
neurophysiological evidence of reconnection of fibers from motor origin
a set of tests evaluating the conductivity of efferent central and peripheral nerve fibers and the muscle response to electrical stimulation, including motor evoked potentials (MEP), electromyography (EMG) and electroneurography (ENG),
Time frame: tested every 3 months for at least 2 years postoperatively
neurophysiological evidence of reconnection of fibers from sensory origin
the electrical perceptual thresholding (EPT) test- evaluating the dermatomal sensation of the upper and lower limbs in the condition of low voltage current application (from 0 to 7-8 mA) Interpretation of the test: any tingling sensation reported by the patient in the previously anesthetic dermatomes, in the condition of current below 4 mA will be considered as essential improvement of skin sensation.
Time frame: tested every 3 months for at least 2 years postoperatively
neurophysiological evidence of reconnection of fibers from vegetative origin
skin sympathetic response (SSR) Electrophysiological study assessing the integrity of the supraspinal autonomic pathways. Is performed on the median and tibial nerves. Test interpretation: any positive vegetative response in the tested paralyzed limbs that was previously absent will be considered as positive outcome.
Time frame: tested every 3 months for at least 2 years postoperatively
improvement of urination registered in the urodynamic study
a test measuring the electrophysiological activity of the bladder muscles and the bladder sensation Test interpretation: Any evidence of bladder detrusor -urethral sphincter synergy, together with the evidence of improved urination will be considered as positive outcome
Time frame: tested every 3 months for at least 2 years postoperatively
evidence regrowth of spinal cord fibers detected on MRI scans, evidence of functional reorganization of the brain detected in advanced MRI protocols; lack of tumorigenesis, spinal cord inflammation, progressive syringomyelia;
evidence of spinal cord fiber reconstitution and brain center reorganization detected on MRI scans, including advanced imaging techniques
Time frame: MRI imaging of the spinal cord and brain will be performed every 3 months in the first year and every 6 months in the second year