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Clinical study of human umbilical cord blood mesenchymal stem cells in the treatment of refractory lupus nephritis

Clinical study of human umbilical cord blood mesenchymal stem cells in the treatment of refractory lupus nephritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17011765
Enrollment
Unknown
Registered
2017-06-26
Start date
2017-08-01
Completion date
Unknown
Last updated
2017-07-03

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

Conditions

lupus nephritis

Interventions

MSCs infusion group:On the basis of conventional doses of corticosteroids + immunosuppressive agents, four 1*10^7/Kg UC MSCs (first, seventh, and six months after the first and seventh days) were admi
control group:Routine dose of glucocorticoid + immunosuppressive agent

Sponsors

Tianjin First Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 70 Years

Inclusion criteria

Inclusion criteria: SLE patients met the following criteria: 1. meet the American College of Rheumatology 1997 revised SLE classification diagnostic criteria, aged 16~70 years old; 2. lupus nephritis (LN), urine protein (24h) = 1000mg/24h; 3. dimensional prednisone = 20mg/d; cyclophosphamide (CTX); 4. CTX total cumulative amount of invalid 8~10g refers to patients before a recent treatment (12~18 months) accumulation, or other immunosuppressive agents (cyclosporine A, azathioprine, mycophenolate mofetil etc) is invalid for 3 months.

Exclusion criteria

Exclusion criteria: The patient had an infection that was not controlled; the patient had one or more organ failure; pregnancy or breast feeding; rejected mesenchymal stem cell transplantation; could not be followed up

Design outcomes

Primary

MeasureTime frame
24H urinary protein quantitation;WBC;PLT;creatinine;SLEDAI score;

Countries

China

Contacts

Public ContactQi Wufang

Tianjin First Central Hospital

13702061222@163.com+86 13702061222

Outcome results

None listed

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