Skip to content

Cancelled by the investigator Clinical study of mesenchymal stem cells in treating severe novel coronavirus pneumonia (COVID-19)

Clinical study of mesenchymal stem cells in treating severe novel coronavirus pneumonia (COVID-19)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030224
Enrollment
Unknown
Registered
2020-02-26
Start date
2020-02-26
Completion date
Unknown
Last updated
2020-03-23

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

Conditions

Novel Coronavirus Pneumonia (COVID-19)

Interventions

1 the critical group :injecting Mesenchymal stem cells
2 the severe group:injecting Mesenchymal stem cells
3 the control group of the critical group:injecting normal saline
4 the control group of the severe group:injecting normal saline

Sponsors

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Female patients aged >=18 years who were of childbearing years were excluded from pregnancy and agreed to use non-drug contraceptive measures during the study period; 2. SARS-CoV-2 nucleic acid test positive; 3. Lung CT examination showed evaluable lesions; 4. Meet the diagnostic criteria for severe or critical illness in the diagnosis and treatment program for new coronavirus pneumonia (trial version 6); 5. Subjects voluntarily participate in the study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Allergy to drugs and excipients used in this study; 2. Pregnant and lactating women and women of child-bearing years did not agree to use contraception during the experiment; 3.Have malignant tumor or hypercoagulant state; 4. Suffer from mental illness and can't cooperate well; 5. Those who have participated in or are participating in clinical trials of other drugs during the course of the disease; 6. Other conditions considered inappropriate for inclusion by the researcher.

Design outcomes

Primary

MeasureTime frame
SP02;lesions of lung CT;temperature;Blood routine;Inflammatory biomarkers;

Secondary

MeasureTime frame
hepatic and renal function;

Countries

China

Contacts

Public ContactChengyun Liu

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

chengyunliu@hust.edu.cn+86 18007117616

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026