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Clinical Trials/NCT01494480
NCT01494480
Unknown
Phase 2

The Clinical Study on the Use of Umbilical Cord Mesenchymal Stem Cells in Amyotrophic Lateral Sclerosis

General Hospital of Chinese Armed Police Forces1 site in 1 country30 target enrollmentMarch 2012

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Amyotrophic Lateral Sclerosis
Sponsor
General Hospital of Chinese Armed Police Forces
Enrollment
30
Locations
1
Primary Endpoint
Nerve functional evaluation
Last Updated
13 years ago

Overview

Brief Summary

Patients with Amyotrophic Lateral Sclerosis (ALS) typically endure a progressive paralysis due to the continued loss of motoneurons that leads them to death in less than 5 years. No treatment has changed its natural history. Intrathecal injection of umbilical cord mesenchymal stem cells can secret trophic factors that keep the motorneurons functional. The investigators have designed a phase I/II clinical trial to check the feasibility of this approach in humans.

Detailed Description

A total of 30 diagnosed ALS patients. The patients would got these symptoms such as gait difficulty and tremor, hand incoordination or speech difficulties.

Registry
clinicaltrials.gov
Start Date
March 2012
End Date
April 2015
Last Updated
13 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
General Hospital of Chinese Armed Police Forces
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Diagnose established following the World Federation of Neurology criteria
  • More than 6 and less than 36 months of evolution of the disease
  • Medullar onset of the disease
  • More than 20 and less than 65 years old
  • Forced Vital Capacity equal or superior to 50%
  • Total time of oxygen saturation \<90% inferior to 2% of the sleeping time
  • Signed informed consent

Exclusion Criteria

  • Neurological or psychiatric concomitant disease
  • Need of parenteral or enteral nutrition through percutaneous endoscopic gastrostomy or nasogastric tube
  • Concomitant systemic disease
  • Treatment with corticosteroids, immunoglobulins or immunosuppressors during the last 12 months
  • Inclusion in other clinical trials
  • Unability to understand the informed consent

Outcomes

Primary Outcomes

Nerve functional evaluation

Time Frame: within one week before,1month,6months,12months and 24months after transplantation

1. Medical Research Council scale:To determine the strength of bilateral little finger abductor muscle and anterior tibial. 2. To evaluate the situation of upper motor neuron impairment through the Ellis reflex scale 3. The severity evaluation: NorrisALS score and ALS functional rating scale, ALSFRS 4. Speed of disease progression by the following formula:Progress rate = (40-ALSFRS score) / course 5. Questionnaires related to sleep, depression (Beck Depression Inventory) (BDI) and memory (Mini Mental State Examination)

Forced vital capacity

Time Frame: within one week before,1month,6months,12months and 24months after transplantation

vital capacity(VC)、forced vital capacity( FVC)、forced expiratory volune(FEV1)、FEV1/FVC、maximal voluntary ventilation(MVV)、peak expiratory flow(PEF)

Secondary Outcomes

  • Blood test(within one week before,1month,6months,12months and 24months after transplantation)
  • Urinal test(within one week before,1month,6months,12months and 24months after transplantation)
  • Electrophysiology examination(within one week before,1month,6months,12months and 24months after transplantation)

Study Sites (1)

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