Safety Study of Endobronchial Transplantation of Autologous Mesenchymal Stem Cells (MSCs) in Emphysema Patients
Primary Purpose
Emphysema
Status
Unknown status
Phase
Phase 1
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
Autologous MSCs transplantation
Sponsored by
About this trial
This is an interventional treatment trial for Emphysema focused on measuring Mesenchymal stem cell, emphysema, lung function
Eligibility Criteria
Inclusion Criteria:
• Inclusion criteria were as follows:
- patients with moderate to severe emphysema that has a FEV1≤50% (approved by HRCT)
- aged less than 70 years
- no tobacco use for at least 12 months before the protocol application
- no serious coronaropathy and/or ventricular dysfunction
- no significant renal illness and/or hepatitis
- EF(ejection fraction)>50%
- Creatinine < 2
- AST, ALT≤ 10 times of its normal basis
Exclusion Criteria:
Exclusion criteria were as follows:
- detected immunosuppressive illnesses
- carrier of known neoplasias
- pregnancy
- limitation in daily physical activities
- known case of diabetic disorders
- modifying in his/her medical treatment regime in the past year
Sites / Locations
- Masih-Daneshvari Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Autologous MSCs transplantation
Arm Description
intra bronchial injection, Autologous MSCs transplantation derived bone marrow, 60millions cells, once
Outcomes
Primary Outcome Measures
forced vital capacity( FVC), forced expiratory volume(FEV1), FEV1/FVC
A pulmonary function test that measures the volume and speed of inhaled air.
A pulmonary function test that measures the volume and speed of exhaled air.
Secondary Outcome Measures
six minute walk test
•A six minute walk test with treadmills
Full Information
NCT ID
NCT01758055
First Posted
November 18, 2012
Last Updated
December 23, 2012
Sponsor
Arda Kiani
Collaborators
Royan Institute
1. Study Identification
Unique Protocol Identification Number
NCT01758055
Brief Title
Safety Study of Endobronchial Transplantation of Autologous Mesenchymal Stem Cells (MSCs) in Emphysema Patients
Official Title
Safety Study of Endobronchial Transplantation of Autologous Mesenchymal Stem Cells Derived Bone Marrow in Patients With Emphysema
Study Type
Interventional
2. Study Status
Record Verification Date
November 2012
Overall Recruitment Status
Unknown status
Study Start Date
December 2012 (undefined)
Primary Completion Date
December 2013 (Anticipated)
Study Completion Date
January 2014 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Arda Kiani
Collaborators
Royan Institute
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is evaluating the safety of endobronchial transplantation of autologous mesenchymal stem cells derived bone marrow in patients with emphysema.
Detailed Description
Chronic obstructive pulmonary disease (COPD) is a worldwide epidemic disease that the global prevalence of it was estimated to be approximately 210 million individuals and accounting for more than three million deaths annually. And currently, it is the fifth chief cause of death in the United State of America. COPD is characterized by chronic, irreversible inflammation of the airways and has two pathologic features, emphysema and bronchiolitis.
The most relevant feature in the lung emphysema is airflow limitation, resulting from the loss of alveolar wall and enlargement of alveolar space distal to the terminal bronchiole. Cigarette and air pollution are the most major factors for developing COPD. Unfortunately, aside from supplemental domiciliary oxygen for the small number of patients who demonstrate resting arterial hypoxemia and smoking cessation for continued smokers, there are no interventions that have been unequivocally shown to prolong survival in patients with COPD. In the preprocessing phase, patients will underwent a complete evaluation of the pulmonary function test with spirometer to measure the FEV1, FVC, FEV1/FVC, cardiac evaluation (clinical examination, six minute walk test, echocardiography TTE(transthoracic echocardiography ), and electrocardiography),chest X-ray, chest computed tomography scan (helical/high resolution),o2 saturation by oximeter, as well as routine laboratory tests (blood gas, urinalysis, coagulation, complete blood count (CBC), blood urea nitrogen, fasting glucose, creatinine, AST(aspartate aminotransferase), ALT(alanine aminotransferase), C-reactive protein, serology for hepatitis B and C, antihuman immunodeficiency virus, and treponemal test for syphilis (FTA-ABS)). The Dyspnea Scale Score test, modified according to the British MMRC, was also conducted, according to Mahler and Wells and Curley.And quality of life measures will assess according to SF-36(Medical Outcomes Study 36-Items Short-Form Health Survey) questioner.
Patients will taken to the operating room, placed in a prone position, and administer a spinal anesthesia. Approximately, 120 mL of bone marrow will aspirated from each puncture and after preparation about 60 million autologous MSCs will transplant by bronchoscopy into the endobronchial of these patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Emphysema
Keywords
Mesenchymal stem cell, emphysema, lung function
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Autologous MSCs transplantation
Arm Type
Experimental
Arm Description
intra bronchial injection, Autologous MSCs transplantation derived bone marrow, 60millions cells, once
Intervention Type
Biological
Intervention Name(s)
Autologous MSCs transplantation
Intervention Description
Autologous mesenchymal stem cells derived bone marrow, bronchoscopy
Primary Outcome Measure Information:
Title
forced vital capacity( FVC), forced expiratory volume(FEV1), FEV1/FVC
Description
A pulmonary function test that measures the volume and speed of inhaled air.
A pulmonary function test that measures the volume and speed of exhaled air.
Time Frame
Baseline and one year after procedure
Secondary Outcome Measure Information:
Title
six minute walk test
Description
•A six minute walk test with treadmills
Time Frame
Baseline and One year after procedure
Other Pre-specified Outcome Measures:
Title
oxygen saturation
Description
•An oximeter test for evaluating the oxygen saturation
Time Frame
Baseline and one year after procedure
Title
Quality of life
Description
•A SF36 quality of life questioner for evaluating the quality of life
Time Frame
Baseline and One year after procedure
Title
DLCO(diffusion capacity of lung for carbon monoxide)
Description
•Body Box device for evaluating diffusing capacity of the lung for carbon monoxide
Time Frame
Baseline and One year after procedure
Title
CT scan
Description
•A CT scan for evaluating the changes
Time Frame
Baseline and One year after procedure
Title
dyspnea score
Description
•A MMRC(modified medical research council) scale for evaluating the dyspnea score
Time Frame
Baseline and One year after procedure
Title
Atrial blood gases test-PaO2(partial pressure of oxygen in blood) , PaCO2(partial pressure of carbon dioxide in blood)
Description
presence of oxygen in blood gases
presence of carbon dioxide in blood gases
Time Frame
Baseline and one year after procedure
Title
Infection
Description
•A CBC test for evaluating the infection
Time Frame
Baseline and one year after procedure
10. Eligibility
Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
• Inclusion criteria were as follows:
patients with moderate to severe emphysema that has a FEV1≤50% (approved by HRCT)
aged less than 70 years
no tobacco use for at least 12 months before the protocol application
no serious coronaropathy and/or ventricular dysfunction
no significant renal illness and/or hepatitis
EF(ejection fraction)>50%
Creatinine < 2
AST, ALT≤ 10 times of its normal basis
Exclusion Criteria:
Exclusion criteria were as follows:
detected immunosuppressive illnesses
carrier of known neoplasias
pregnancy
limitation in daily physical activities
known case of diabetic disorders
modifying in his/her medical treatment regime in the past year
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Arda Kiani, MD,PULMONO
Phone
0098-021-27122171
Email
Kiani@nritld.ac.ir
First Name & Middle Initial & Last Name or Official Title & Degree
Naser Aghdami, MD, PHD
Phone
0098-021-22172330
Email
nasser.aghdami@royaninstitute.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Arda Kiani, MD, pulmono
Organizational Affiliation
Tracheal Diseases Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Naser Aghdami, MD,PHD
Organizational Affiliation
Department of Regenerative Biomedicine and cell therapy,Cell science Research Center,Royan Institute for Stem Cell Biology and Technology,ACER,Tehran,Iran
Official's Role
Study Director
Facility Information:
Facility Name
Masih-Daneshvari Hospital
City
Tehran
ZIP/Postal Code
021
Country
Iran, Islamic Republic of
Facility Contact:
First Name & Middle Initial & Last Name & Degree
ARDA KIANI, MD,PULMONO
Phone
0098-021-27122171
Email
KIANI@NRITLD.AC.IR
First Name & Middle Initial & Last Name & Degree
PARITASH TAHMASEB POUR, MD
Phone
0098-09125037861
Email
PARITASH_T@YAHOO.COM
First Name & Middle Initial & Last Name & Degree
Paritash Tahmaseb pour, MD
First Name & Middle Initial & Last Name & Degree
Hoda Madani, MD
12. IPD Sharing Statement
Learn more about this trial
Safety Study of Endobronchial Transplantation of Autologous Mesenchymal Stem Cells (MSCs) in Emphysema Patients
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