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Severe novel coronavirus pneumonia (COVID-19) patients treated with ruxolitinib in combination with mesenchymal stem cells: a prospective, single blind, randomized controlled clinical trial

Severe novel coronavirus pneumonia (COVID-19) patients treated with ruxolitinib in combination with mesenchymal stem cells: a prospective, single blind, randomized controlled clinical trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000029580
Enrollment
Unknown
Registered
2020-02-05
Start date
2020-01-31
Completion date
Unknown
Last updated
2020-03-09

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

Experimental group:Ruxolitinib combined with mesenchymal stem cell
control group: Routine treatment

Sponsors

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

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years and <= 75 years; 2. Patients clinically diagnosed as novel coronavirus infection; or with positive serum antibodies (IgM or IgG); or with novel coronavirus infection confirmed by PCR; 3. Severe/critical patients.

Exclusion criteria

Exclusion criteria: 1. Patients with other malignant tumors requiring treatment; 2. Severe cardiovascular and metabolic diseases beyond the control of combination with other drugs 3. Patients with clinical symptoms of brain dysfunction or serious mental illness who cannot understand or follow the study protocol; 4. Endotracheal intubation with invasive ventilation; 5. Patients who cannot guarantee completion of necessary treatment plan and follow-up observation; 6. Women of child-bearing age who are positive in pregnancy test or do not stop breastfeeding in lactation period; 7. Patients with other infections at the time of enrollment; 8. Other circumstances that prevent the protocol from proceeding safely.

Design outcomes

Primary

MeasureTime frame
Safety;

Countries

China

Contacts

Public ContactJianfeng Zhou

Department of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology

zhougene@medmail.com.cn+86 027 83665506

Outcome results

None listed

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