Intrathecal Autologous ADRC Treatment of Autoimmune Refractory Epilepsy
NCT ID: NCT03676569
Last Updated: 2020-04-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1
6 participants
INTERVENTIONAL
2015-11-15
2019-04-14
Brief Summary
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Study protocol:
Intrathecal infusions of autologous ADRC obtained after liposuction followed by isolation by Cytori system will be performed. Procedure will be repeated 3 times every 3 months in each patient. Neurological status, brain MRI, cognitive function and antiepileptic effect will be supervised during 24 months.
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Detailed Description
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In patients who were diagnosed with autoimmune drug-resistant epilepsy and have met the set criteria and qualified to take part in the examination, after a formal written consent of their parents at the Clinic of Child Neurology IMC neurological examination, routine laboratory tests, EEG and neuropsychological assessment will be performed. ADRC will be obtained after liposuction and isolation with Cytori system.
Before intrathecal transplantation of ADRC suspension ( 5 ml), cerebrospinal fluid will be collected for evaluation of origin protein level, oligoclonal bands, the IgG index as well as GluR3, VGKC complex/LGI1, GM1, NT-3, GAD, and NMDAR antibodies. At the same time there will be an intake of 5ml of serum to evaluate levels of immunoglobulins IgA, IgM and IgG.
Procedure will be repeated 3 times every 3 months in each patient. Neurological status, brain MRI, cognitive function and antiepileptic effect will be supervised during 24 months.
Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Experimental group
Autologous ADRC transplantation in autoimmune refractory epilepsy
ADRC transplantation in autoimmune refractory epilepsy
Interventions
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ADRC transplantation in autoimmune refractory epilepsy
Eligibility Criteria
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Inclusion Criteria
* Children between 3 and 18 years old
* Presence of antineuronal antibody in serum or CSF
* Rasmussen encephalitis (proven cellular immunity pathogenesis)
* Probable autoimmune pathogenesis (autoimmune diseases in family, febrile infection associated refractory epilepsy)
* Willing and able to provide written informed consent (patient or legal guardian)
Exclusion Criteria
* Neoplastic disease
* Active inflammatory process at the time of recruitment
* Coagulation disorder
* Status epilepticus
* Participation in another clinical trial
* Lack of willingness and ability to provide written informed consent
ALL
No
Sponsors
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Institute of Mother and Child, Warsaw, Poland
OTHER
Mossakowski Medical Research Centre Polish Academy of Sciences
OTHER
Responsible Party
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Anna Sarnowska
M.D., Ph.D.; Head of Translative Platform for Regenerative Medicine MRC Mossakowski PAS
Principal Investigators
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Dorota Antczak-Marach, M.D.
Role: PRINCIPAL_INVESTIGATOR
Institute of Mother and Child
Ewa Sawicka, Prof.
Role: PRINCIPAL_INVESTIGATOR
Institute of Mother and Child
References
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Szczepanik E, Mierzewska H, Antczak-Marach D, Figiel-Dabrowska A, Terczynska I, Tryfon J, Krzesniak N, Noszczyk BH, Sawicka E, Domanska-Janik K, Sarnowska A. Intrathecal Infusion of Autologous Adipose-Derived Regenerative Cells in Autoimmune Refractory Epilepsy: Evaluation of Safety and Efficacy. Stem Cells Int. 2020 Jan 3;2020:7104243. doi: 10.1155/2020/7104243. eCollection 2020.
Other Identifiers
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17/2014 IMiD
Identifier Type: -
Identifier Source: org_study_id
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