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Adipose Derived Stem Cells Transplantation for Chronic Obstructive Pulmonary Disease

Evaluation of Safety and Efficacy of Autologous Adipose Derived Stem Cells Transplantation for Chronic Obstructive Pulmonary Disease

Status
UNKNOWN
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02645305
Enrollment
20
Registered
2016-01-01
Start date
2015-06-30
Completion date
2016-12-31
Last updated
2016-01-01

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

Conditions

COPD

Keywords

Safety and Efficacy, Adipose stem cells, Stem Cell therapy

Brief summary

Chronic obstructive pulmonary disease (COPD) is the name for a collection of lung diseases including chronic bronchitis, emphysema and chronic obstructive airways disease. People with COPD have difficulties breathing, primarily due to the narrowing of their airways, this is called airflow obstruction. Some preclinical evaluations showed that COPD is closely related to chronic inflammation; therefore, this study aimed to use adipose-derived stem cells (ADSCs) in the form of non-expanded culture - that usually names as a stromal vascular fraction (SVF) in combination with activated platelet rich plasma (PRP) to treat this disease. Both SVF and PRP are autologous sources that obtained from adipose tissue and peripheral blood, respectively. This mixture is intravenously transfused into the patients.

Interventions

Adipose derived stem cells that are isolated from adipose tissue are mesenchymal stem cells with high immune modulation capacity. Therefore, they can effectively modulate the immune system.

Sponsors

Van Hanh General Hospital
CollaboratorOTHER
Nguyen Tri Phuong Hospital, Ho Chi Minh city, Viet Nam
CollaboratorUNKNOWN
GeneWorld Ltd Co, Ho Chi Minh city, Viet Nam
CollaboratorUNKNOWN
University of Science Ho Chi Minh City
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Age 40 to 80, inclusive * A prior diagnosis of moderate to severe COPD * GOLD IIa, III, IV

Exclusion criteria

* Pregnant or lactating * Life expectancy \< 6 months due to concomitant illnesses. * Exposure to any investigational drug or procedure within 1 month prior to study entry or enrolled in a concurrent study that may confound results of this study. * Any illness which, in the Investigators judgment, will interfere with the patient's ability to comply with the protocol, compromise patient safety, or interfere with the interpretation of study results * Subjects on chronic immunosuppressive or chemotherapeutic therapy * Known drug or alcohol dependence or any other factors which will interfere with the study conduct or interpretation of the results or who in the opinion of the investigator are not suitable to participate. * Subjects with Alpha-1 antitrypsin deficiency (an inherited disorder that can cause lung disease and liver disease). * Unwilling and/or not able to give written consent * Patient is positive for hepatitis (past history of Hepatitis A is allowed) * Any medical condition, which in the opinion of the clinical investigator, would interfere with the treatment or outcome of the patient * Cerebral aneurysm clips

Design outcomes

Primary

MeasureTime frameDescription
SGOT1 monthThe blood SGOT levels are thus elevated with liver damage
SGPT1 monthThe blood SGPT levels are thus elevated with liver damage

Secondary

MeasureTime frameDescription
Respiration rate1 month, 6 months, 12 months
6 min walk test1 month, 6 months, 12 months
rates of panic attacks1 month, 6 months, 12 months
CRP concentration6 months, 12 monthsThe CRP concentration in the patients were evaluated before and after treatment for 6 and 12 months

Countries

Vietnam

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026