Autologous Mesenchymal Stem Cells Transplantation in Cervical Chronic and Complete Spinal Cord Injury
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|ClinicalTrials.gov Identifier: NCT02574572|
Recruitment Status : Recruiting
First Posted : October 14, 2015
Last Update Posted : November 28, 2017
|Condition or disease||Intervention/treatment||Phase|
|Spinal Cord Injury||Biological: Autologous mesenchymal cells transplantation||Phase 1|
This is a pilot, phase I study, in a prospective cohort. The study population will consist of 10 patients who had spinal cord injury for at least 12 months, with cervical chronic and complete spinal cord injury, ASIA grade A.
A practitioner, a surgeon and a nurse will review the medical records of the patients to determine the presence / absence of inclusion / exclusion criteria. If the patient is a potential candidate for the study, an interview will be scheduled to review and confirm his/her eligibility.
Patients will undergo a series of clinical and neurological assessments and will also be submitted to the following procedures:
- Cell blood count;
- Biochemical analysis (measurement of electrolytes - sodium, potassium, magnesium);
- Renal function tests (urea and creatinine);
- Liver function tests;
- Coagulation profile;
- Metabolic profile (glucose, total cholesterol and fractions);
- Urine summary and culture;
- Serology required for blood transfusion and marrow transplant in Brazil;
- Chest X-Ray;
- Bone densitometry;
- Urodynamic studies;
- Somatosensory evoked potential;
- Computed tomography of thoracic and lumbar spine;
- Magnetic resonance imaging of the thoracic and lumbar spine.
Also as part of the preoperative evaluation, the patients will respond to questions from the SF (Short Form) -36 questionnaire (for assessment of quality of life) and the questionnaires for the assessment of neuropathic pain.
Clinical follow-up will be kept for patients who suspend their participation in the study for any adverse event and / or laboratory abnormality, or for the patient's own desire, following insurance protocols. In addition to the clinical and surgical follow-up, specific medical care will be offered to patients who experience adverse events, until stabilization of the patient, even if the target date for completion of the study has been exceeded.
The candidates included in the study will be asked to voluntarily participate and give their informed written consent.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||10 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Evaluation of the Safety and Potential Effectiveness of Autologous Mesenchymal Stem Cells Transplantation in Subjects With Cervical Chronic and Complete Spinal Cord Injury|
|Actual Study Start Date :||September 6, 2017|
|Estimated Primary Completion Date :||December 31, 2019|
|Estimated Study Completion Date :||June 30, 2020|
Experimental: Single group
Patients with spinal cord injury that will undergo laminectomy and autologous mesenchymal cells intralesional injection
Biological: Autologous mesenchymal cells transplantation
All patients will undergo laminectomy and autologous mesenchymal cells injection into the lesion area.
- Number of participants with treatment-related adverse events as assessed by magnetic resonance imaging [ Time Frame: 12 months ]
- Functional improvement in ASIA (American Spinal Injury Association) grade [ Time Frame: 12 months ]The investigators will evaluate the conversion rate from ASIA A to B or C in 12 months.
- Functional improvement regarding the AIS (ASIA Impairment Scale) scores (light touch, pin prik and motor force) [ Time Frame: 12 months ]AIS (ASIA Improvement Scale) degree on the ASIA score will be assessed in order to evaluate sensitivity and motor force in 12 months.
- Improvements in sensorial mapping and neuropathic pain [ Time Frame: 12 months ]The patients will be submitted to specific questionnaires and clinical examinations in order to evaluate improvements in sensorial mapping and neuropathic pain.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02574572
|Contact: Ricardo Ribeiro-dos-Santos, PhDfirstname.lastname@example.org|
|Hospital São Rafael||Recruiting|
|Salvador, Bahia, Brazil, 41253190|
|Contact: Ticiana F Larocca, MD, MSc +557132816489 email@example.com|
|Contact: Carolina T Macedo, MD, MSc +557132816489 firstname.lastname@example.org|
|Principal Investigator:||Ricardo Ribeiro-dos-Santos, PhD||Hospital São Rafael|
|Study Director:||Milena BP Soares, PhD||Hospital São Rafael|
|Study Chair:||Bruno SF de Souza, MD, Msc||Hospital São Rafael|
|Study Chair:||Ticiana F Larocca, MD, Msc||Hospital São Rafael|
|Study Chair:||Rodrigo L Alves, MD, PhD||Hospital São Rafael|
|Study Chair:||Carolina T Macedo, MD, MSc||Hospital São Rafael|
|Study Chair:||André C Matos, MD||Hospital São Rafael|
|Study Chair:||Cristiane F Villarreal, PhD||Fundação Oswaldo Cruz|
|Study Chair:||Antônio Olímpio S Moura, MD||Hospital São Rafael|
|Study Chair:||Eduardo Brazão, MD||Hospital São Rafael|
|Study Chair:||Kátia N Silva, MSc||Hospital São Rafael|
|Study Chair:||Daniela N Silva, MSc||Hospital São Rafael|
|Study Chair:||Clarissa LM de Souza, MD||Hospital São Rafael|