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NCT06280092LeállítvaKorai 1. fázis

Allogenic Adipose-derived Mesenchymal Stem Cells(AMSCs) for Epilepsy During Deep Brain Stimulation(DBS) Surgery

A Pilot Study to Evaluate the Feasibility and Safety of Allogenic Adipose-derived Mesenchymal Stem Cells(AMSCs) for Epilepsy During Deep Brain Stimulation(DBS) Surgery

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. szept. 8.

Megadott ok: PI has passed away

Rövid összefoglaló (regiszter, angolul)

This study is a non-randomized, open label, phase 1 clinical trial to evaluate the fesibility and safety of intrathalamic delivery of MSCs during standard of care DBS surgery for epilepsy. Subjects will be screened at our outpatient clinic and interested qualified subjects will be consented and offered participation in this trial. Once consent has been obtained, patients will undergo a standard preoperative evaluation which includes baseline laboratory values and a high-definition MRI. Patients will then undergo a stereotactic procedure for bilateral thalamic implantation of DBS leads through the ClearPoint® system. After the thalamic target for DBS is identified, cells will be infused directly into the anterior nucleus of the thalamus previous to lead implantation. Patients will be followed in the outpatient setting for up to a year after therapy application. Surgical, clinical, and radiographic data will be obtained during these visits

Állapot (regiszter)
Leállítva
Fázis (regiszter)
Korai 1. fázis
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
1 (tényleges)
Első benyújtás
2024. febr. 20.
Kezdés
2024. dec. 23.
Elsődleges befejezés
2026. szept. 3.
Fő szponzor
Mayo Clinic
Betegségek
Epilepszia
NCT-szám
NCT06280092

Ki nem vehet részt

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Korábbi kezelés

  • Patients who have undergone a prior intracranial procedure for epilepsy.
  • Subjects allergic to any component of the investigational product.

Más betegség

  • History of cancer not in remission for at least 5 years.
  • History of diabetes, chronic renal failure, or other significant underlying medical or ----immunosuppressive conditions.
  • History of drug or alcohol abuse.

Életkor

  • Subjects > 75 years of age.

Egyéb

  • Patients with an intracranial tumor.
  • Confirmed pregnancy.
  • Cognitively impaired adults.

Kiket keres a vizsgálat

  • Participants ≥ 18 years of age.
  • Participants with Drug Resistance Epilepsy as defined by the ILAE5.
  • Participants undergoing bilateral implantation of DBS leads into the anterior nucleus of the thalamus.
  • Adequate organ function as assessed by the following laboratory values within 3 weeks prior to admission to the study:
  • Serum creatinine and urea < 2 times the upper limit of normal;
  • ALT, AST and alkaline phosphatase < 3 times the upper limit of normal, and bilirubin < 2.5 mg/dL;
  • Prothrombin time ≤ 1.5 times upper limit of normal;
  • INR and PTT ≤ 1.5 times the upper limit of normal;
  • Hemoglobin ≥ 9 g/dL;
  • Platelets ≥ 100 x 10\^9/L;
  • Absolute Neutrophil Count (ANC) ≥ 1.5 x 10\^9/L.
  • Patient or legal guardian is able to fully understand and provide written and verbal consent for the protocol.
  • Patient is a candidate for ANT DBS based on the following criteria established by the American Society for Stereotactic and Functional Neurosurgeons:
  • Confirmed diagnosis of epilepsy by an epileptologist with focal-onset seizures, with or without generalization;
  • Failure to adequately control seizures after two (or more) appropriate and adequately-dosed anti-seizure medications;
  • Either partial-onset seizures with a localized onset in a region not amenable to resection or following failed resective surgery or focal-onset seizures with distributed or unclear onset zone.

Életkor a regiszterben: 18 év – 75 év · Nem: nők és férfiak · Egészséges önkénteseket nem fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (1)

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HelyszínVárosOrszágHelyszín állapota
Mayo ClinicJacksonvilleEgyesült ÁllamokIsmeretlen állapot

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