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Safety and Efficacy Study of Umbilical Cord-Derived Mesenchymal Stem Cells for Rheumatoid Arthritis (RA)

Safety and Efficacy Study of Umbilical Cord-Derived Mesenchymal Stem Cells for Rheumatoid Arthritis (RA)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-16008770
Enrollment
Unknown
Registered
2016-07-03
Start date
2016-05-01
Completion date
Unknown
Last updated
2018-02-12

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

Conditions

rheumatoid arthritis

Interventions

treatment group:hUC-MSCs

Sponsors

Research Institute of Surgery, Daping Hospital, Third Military Medical University, Chongqing
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients must sign an informed consent indicating that they are aware of the investigational nature of the study in keeping with the policy of the hospital; 2. Patients of RA, to be aged 18 years to 65 years old; 3. All patients fulfilled the classification criteria (ACR21987) for rheumatoid arthritis; 4. All patients fulfilled hormone-dependent or through formal use of methotrexate / leflunomide / hydroxychloroquine sulfate / sulfasalazine and / or at least one kind of TNF-a inhibitor, is still high disease activity or can not be tolerated.

Exclusion criteria

Exclusion criteria: 1. Patients with uncorrected disease, such as advanced cancer or other terminal illness, the prospective survival period less than 28 days; 2. Patients in the foreseeable dying state; 3. Have the bone marrow, lungs, liver, pancreas, or small bowel transplantation history; 4. Have severe heart and lung failure, or irreversible damage or failure of other major organs; 5. Uncontrolled infection; 6. Patient participating or having participated in a clinical trial with another investigational drug Within 30 days before the start of this clinical trial; 7. Patient is pregnant or nursing; 8. History of patient is allergic to biological products; 9. HIV infected associated with the recent CD4+ cell count =50/mm3; 10. viral hepatitis.

Design outcomes

Primary

MeasureTime frame
DAS28;HAQ??;CRP;ESR;

Countries

China

Contacts

Public ContactXiang Xu

Department of Rheumatology and Immunology, Daping Hospital, Third Military Medical University, Chongqing

xiangxu@ymail.com+86 13637843870

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 6, 2026