Clinical Study of Adipose Derived Mesenchymal Stem Cells for Treatment of Pulmonary Arterial Hypertension

Pulmonary Hypertension Clinical Trial

Official title:

Safety and Efficacy of Transplantation of Adipose Derived Mesenchymal Stem Cells to Treat Pulmonary Arterial Hypertension

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04055415
• Other study ID #: mashengjun2
• Status: Recruiting
• Phase: Phase 1/Phase 2
• Start date: August 1, 2019
• Est. completion date: February 1, 2021

Study information

• Verified date: August 2019
• Source: Liaocheng People's Hospital
• Contact: Shaoda Ren, Ph.D.
• Phone: 86-0635-8272202
• Email: zslrsd[@]163.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Pulmonary arterial hypertension is a disease characterised by pathological changes in the pulmonary arteries leading to a progressive increase in pulmonary vascular resistance and pulmonary artery pressure. Right ventricular failure is the main cause of death in patients with pulmonary arterial hypertension, and the ability of the right ventricle to adapt to the progressive increase in pulmonary vascular resistance associated with changes to the pulmonary vasculature in pulmonary arterial hypertension is the main determinant of a patient's functional capacity and survival.Mesenchymal stem cells (MSCs)are a subset of adult stem cells residing in many tissues, including bone marrow(BM), adipose tissue, umbilical cord blood. Recent experimental findings have shown the ability of MSCs to home to damaged tissues and to produce paracrine factors with anti-inflammatory properties, potentially resulting in reduction of inflammation and functional recovery of the damaged tissues.It was found that MSCs can significantly improve the pulmonary hemodynamics, lung tissue gross and decrease the pulmonary artery pressure, middle artery thickness and right cardiac hypertrophy by intravenous injection.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: February 1, 2021
• Est. primary completion date: August 1, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years to 75 Years

Eligibility

Inclusion Criteria:

(1)40-75years (2)Male or female (3)The patients that COPD with moderate to severe pulmonary hypertension (pulmonary systolic pressure more than 40mmHg)in relatively stable period (4)To preliminary assess the Patients'lifetime have more than 6 months (5)According to the researchers' judgment, they can abide by the research protocol or Volunteer to participate in the clinical study, understand the study procedure and sign the informed consent in person.

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Exclusion Criteria:

1. Patients with acute myocardial infarction and cardiac surgery in the past 1 month

2. Surgery may be required within 8 weeks

3. patients with prior pneumonectomy or having acute, chronic pulmonary embolism or other serious pulmonary diseases

4. Having a history of malignant tumor

5. Participated in other clinical investigators in the last 6 months

6. To allergic to penicillin, gentamicin, aminoglycoside, human serum albumin and DMEM medium

7. A woman who is planning to pregnancy, gestation, or lactation

8. Other reasons caused Pulmonary hypertension and heart failure caused by other causes;Severe liver and kidney failure;Autoimmune diseases;Patients with infectious diseases

9. According toThe researchers' judgments, there are concomitant diseases that seriously endanger the safety of the subjects or affect the completion of the study

10. According to the researcher's judgment, this study is not suitable for other conditions -

Related Conditions & MeSH terms

• Familial Primary Pulmonary Hypertension
• Hypertension
• Hypertension, Pulmonary
• Pulmonary Hypertension

Intervention

Biological:
• adipose derived mesenchymal stem cells
The MSCs of 1×10*6/kg will be given in Central venous catheterization for injection at a total 100 ml (2) the experimental group was treated with conventional drug and adipose mesenchymal stem cell injection, and adipose MSCs were treated with central venous catheterization. The injection cycle was once every week of two times.Injection dose: 1×106 /kg.

Drug:
• Conventional drug therapy(expectorant,bronchodilator)
Conventional drug therapy(expectorant,bronchodilator)

Locations

Country	Name	City	State
China	Liaocheng city people's hospital	Liaocheng	Shandong

Sponsors (1)

Lead Sponsor	Collaborator
Liaocheng People's Hospital

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Pulmonary Vascular Resistance from Baseline		Baseline, 4, 12 and 24 weeks
Secondary	Change from Baseline in Participant Quality of Life Using the SF-36	Eight scale scores are derived from responses to the 36 items of the SF-36 questionnaire which are combined to produce the Physical Component Score and the Mental Component Score. The Physical Component Score is based on the Physical Functioning Scale (10 items), the Role-Physical Scale (4 items), the Bodily Pain Scale (2 items), and the General Health Scale (5 items). The Mental Component Score is based upon the Vitality Scale (4 items), the Social Functioning Scale (2 items), the Role-Emotional Scale (3 items) and the Mental Health Scale (5 items). Each component score is transformed into a 0-100 scale, with higher numbers indicating greater quality of life.	Baseline, 4, 12 and 24 weeks
Secondary	Change in Plasma NT-pro-BNP levels	Plasma NT-proBNP concentration is a useful biomarker for PAH as it is associated with changes in right heart morphology and function.	Baseline, 4, 12 and 24 weeks
Secondary	Change in the IL-1ß, IL-6, PGE-2, TGF-ß, TNF-a and IGF-1 (ng/ul)	To assess pre-specified laboratory assessment for change over time with treatment	Baseline, 4, 12 and 24 weeks
Secondary	Incidence of Treatment Adverse	An AE was any untoward medical occurrence in a participant	Baseline, 4, 12 and 24 weeks
Secondary	Change in Six Minute Walk distance	The 6MWD is a 6 minute walk test. This test, a measure of exercise capacity, assesses the distance that a subject can walk in a period of 6 minutes	Baseline, 4, 12 and 24 weeks