Skip to content

Clinical study for the efficacy of Mesenchymal stem cells (MSC) in the treatment of severe novel coronavirus pneumonia (COVID-19)

Clinical study on the efficacy of Mesenchymal stem cells (MSC) in the treatment of severe novel coronavirus pneumonia (COVID-19)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030835
Enrollment
Unknown
Registered
2020-03-15
Start date
2020-02-14
Completion date
Unknown
Last updated
2020-03-16

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

High dose group:routine treatment + MSc (2 x10^6 / kg / time)
Low dose group:routine treatment + MSc (1x10^6 / kg / time)

Sponsors

the First Affiliated Hospital of Xinxiang Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Male or female patients aged 16-75 years; 2. Willing to sign informed consent; 3. novel coronavirus novel coronavirus is highly novel correlate with the novel coronavirus, based on the standard of suspected cases of new coronavirus infection, real-time fluorescence RT-PCR detection of new coronavirus nucleic acid positive, and sequencing of the virus gene; 4. novel coronavirus pneumonia novel coronavirus infection was diagnosed according to the new coronavirus pneumonia diagnosis and treatment plan (trial version sixth). Severe pneumonia is defined by compliance with any of the following: (1) Dyspnea, RR >=30 times / min; (2) At rest, the oxygen saturation <=93%; (3) PaO2 / FiO2 <=300MMHG (lmmhg = o.133kpa). Pa02 / fi02 should be corrected according to the formula: PaO2 / FiO2 x[atmospheric pressure (mmHg) / 760] The pulmonary imaging showed that the lesions progressed more than 50% within 24-48 hours, and the patients were managed as severe.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. Patients with malignant tumor, other serious systemic diseases and psychosis; 3. Patients who have recently or are participating in other clinical trials; 4. There was evidence of drug addiction within one year before the trial; 5. Inability or unwillingness to provide informed consent or comply with test requirements; 6. Combined with HIV, tuberculosis, influenza virus, adenovirus and other respiratory tract infection virus infection; 7. Other conditions judged by the researcher as unsuitable for participating in the clinical study.

Design outcomes

Secondary

MeasureTime frame
C-reactive protein;Detection of lymphocyte subsets;Procalcitonin;Routine blood test;Chest CT;cytokine;Blood biochemistry;

Countries

China

Contacts

Public ContactDou Qifeng

the First Affiliated Hospital of Xinxiang Medical University

douqifeng@126.com+86 13503735556

Outcome results

None listed

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