search
Back to results

Intraventricular Transplantation of Mesenchymal Stem Cell in Patients With ALS

Primary Purpose

Amyotrophic Lateral Sclerosis

Status
Withdrawn
Phase
Phase 1
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
Intraventricular injection
Sponsored by
Royan Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Amyotrophic Lateral Sclerosis focused on measuring mesenchymal stem cell intraventricular injection ALS

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age:18-65
  • both gender
  • duration of disease<2 years
  • FVC>40% ALS-FRS>26

Exclusion Criteria:

  • neurological and psychiatric concomitant disease
  • concomitant systemic disease
  • treatment with corticosteroid,Ig,immunosuppressive during 12 months.

Sites / Locations

  • Royan Institute

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

stem cell recipient

Arm Description

The patients who underwent mesenchymal stem cell transplantation.

Outcomes

Primary Outcome Measures

fever
evaluation the rate of fever 48hours after stem cell injection
unconsciousness
evaluation the rate of unconsciousness during 6months after stem cell injection.
brain hematoma
Evaluation the rate of hematoma 48hours after stem cell injection.
vomiting
evaluation the rate of vomiting 48hours after stem cell injection.

Secondary Outcome Measures

ALS-FRS
evaluation the improvement of ALS-FRS 6months after stem cell injection.
EMG-NCV
evaluation the improvement of EMG-NCV after stem cell injection.

Full Information

First Posted
December 29, 2012
Last Updated
December 31, 2015
Sponsor
Royan Institute
search

1. Study Identification

Unique Protocol Identification Number
NCT01759784
Brief Title
Intraventricular Transplantation of Mesenchymal Stem Cell in Patients With ALS
Official Title
Safety of Intraventricular Injection of Bone Marrow Derived Mesenchymal Stem Cell in Patients With ALS
Study Type
Interventional

2. Study Status

Record Verification Date
May 2012
Overall Recruitment Status
Withdrawn
Why Stopped
The stereotaxis can be threatful for the patients because of respiratory insufficiency
Study Start Date
March 2014 (undefined)
Primary Completion Date
March 2017 (Anticipated)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Royan Institute

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
ALS is a debilitating disease with varied etiology characterized by rapidly progressive weakness, muscle atrophy and fasciculations, muscle spasticity, difficulty speaking (dysarthria), difficulty swallowing (dysphagia), and difficulty breathing (dyspnea). ALS is the most common of the five motor neuron diseases.Riluzole (Rilutek) is the only treatment that has been found to improve survival but only to a modest extent. It lengthens survival by several months, and may have a greater survival benefit for those with a bulbar onset. It also extends the time before a person needs ventilation support.Stem cell transplantation is a new hopeful way to improve the patients conditions and reduce the period of disabilities.
Detailed Description
In this study our purpose is to evaluate the safety of intraventricular injection of bone marrow derived mesenchymal stem cell.the patients who are eligible,underwent bone marrow aspiration.after cell separation and preparation,the patients underwent mesenchymal stem cell intraventricular injection by stereotaxis.after injection he will be under observed in ICU to monitor the adverse events(allergic and neurological side effects).patients are followed 1th,3th ,6th and 12 months after injection and each time these parameters are checked:ALS-FRS,EMG-NCV,FVC,side effect check list.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Amyotrophic Lateral Sclerosis
Keywords
mesenchymal stem cell intraventricular injection ALS

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
stem cell recipient
Arm Type
Experimental
Arm Description
The patients who underwent mesenchymal stem cell transplantation.
Intervention Type
Biological
Intervention Name(s)
Intraventricular injection
Other Intervention Name(s)
intraventricular injection of mesenchymal stem cell by stereotaxis
Intervention Description
intraventricular injection of mesenchymal stem cell by stereo taxi in patients with ALS
Primary Outcome Measure Information:
Title
fever
Description
evaluation the rate of fever 48hours after stem cell injection
Time Frame
48hours
Title
unconsciousness
Description
evaluation the rate of unconsciousness during 6months after stem cell injection.
Time Frame
6months
Title
brain hematoma
Description
Evaluation the rate of hematoma 48hours after stem cell injection.
Time Frame
48hours
Title
vomiting
Description
evaluation the rate of vomiting 48hours after stem cell injection.
Time Frame
48hours
Secondary Outcome Measure Information:
Title
ALS-FRS
Description
evaluation the improvement of ALS-FRS 6months after stem cell injection.
Time Frame
6months
Title
EMG-NCV
Description
evaluation the improvement of EMG-NCV after stem cell injection.
Time Frame
6months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age:18-65 both gender duration of disease<2 years FVC>40% ALS-FRS>26 Exclusion Criteria: neurological and psychiatric concomitant disease concomitant systemic disease treatment with corticosteroid,Ig,immunosuppressive during 12 months.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hamid Gourabi, PhD
Organizational Affiliation
Head of Royan Institute
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Nasser Aghdami, MD,PhD
Organizational Affiliation
Head of Royan department of degenerative medicine,Head of Royan celltherapy center
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Ali Reza Zali, MD
Organizational Affiliation
Head of Neurosurgery research center of Shahid Beheshti University
Official's Role
Study Director
Facility Information:
Facility Name
Royan Institute
City
Tehran
Country
Iran, Islamic Republic of

12. IPD Sharing Statement

Links:
URL
http://Royaninstitute.org
Description
Related Info

Learn more about this trial

Intraventricular Transplantation of Mesenchymal Stem Cell in Patients With ALS

We'll reach out to this number within 24 hrs