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Clinical study of autologous adipose derived stromal vascular fraction (SVF) in the treatment of motor neuron disease

Clinical study of autologous adipose derived stromal vascular fraction (SVF) in the treatment of motor neuron disease

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091754
Enrollment
Unknown
Registered
2024-11-02
Start date
2024-11-02
Completion date
Unknown
Last updated
2024-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Motor neuron disease

Interventions

SVF treatment group1:Dose group 1: Intravenous infusion of autologous fat derived vascular matrix fraction (SVF) 0.5 × 106/kg
SVF treatment group2:Dose group 2: Intravenous infusion of autologous fat derived vascular matrix fraction (SVF) 1 × 106/kg
SVF treatment group3:Dose group 3: Intravenous infusion of autologous fat derived vascular matrix fraction (SVF) 2 × 106/kg

Sponsors

Suzhou Science & Technology Town Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? Meets the clinical and neurophysiological diagnostic criteria for revised El Escorial motor neuron disease; ? There is no structural damage to the brain and cervical spinal cord, and there is no corresponding manifestation on neuroimaging; ? Forced lung capacity greater than 30%; ? At least have basic nutritional status, with a body mass index of at least 18.5kg/m2; ? The patient and/or family members sign on the informed consent form.

Exclusion criteria

Exclusion criteria: ? Severe medullary damage with forced lung capacity less than 30%; ? Malnutrition, with a body mass index less than 18.5kg/m2; ? Tracheostomy has been performed; ? Exclude patients with a history of mental illness (such as schizophrenia); ? Has a history of systemic diseases. For example, malignant tumors, cardiovascular diseases (including asymptomatic hypertensive heart disease, arrhythmia, ischemic heart disease), stroke, and abnormal coagulation function; ? Cervical spondylosis or other diseases indicated by neuroimaging that may cause clinical symptoms of ALS; ? Stimulate the presence of metal in the local area; ? Serious abnormalities in hearing and vision; ? Skull injury or loss; ? There are contraindications for magnetic resonance imaging examination.

Design outcomes

Primary

MeasureTime frame
The ALS functional rating scale (ALSFRS-R) scores for neurological examination and revision were evaluated before and after treatment, as well as at 1 and 3 months after treatment.;

Secondary

MeasureTime frame
manual muscle strength,MMT;Comprehensive neurophysiological examination;

Countries

China

Contacts

Public ContactJingwei Li

Suzhou Science & Technology Town Hospital

ljw323@yeah.net+86 136 7515 8558

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 2, 2026