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Efficacy of etoposide in Conventional Treatment–Refractory Adult-Onset Still's Disease

Efficacy of etoposide in Conventional Treatment–Refractory Adult-Onset Still's Disease

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17013144
Enrollment
Unknown
Registered
2017-10-28
Start date
2017-11-01
Completion date
Unknown
Last updated
2017-11-06

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

Conditions

Adult-Onset Still's Disease

Interventions

1:Etoposide

Sponsors

Department of Rheumatology, Renji Hospital South Campus, School of Medicine, Shanghai JiaoTong University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: AOSD was diagnosed according to the criteria described by Yamaguchi et al; All patients had previously received standard synthetic immunosuppressive drugs and in some cases other biologic agents; Written informed consent form approved for each hospital was requested and obtained from each patient prior to the onset of etoposide treatment.;Inclusion criteria: AOSD was diagnosed according to the criteria described by Yamaguchi et al; All patients had previously received standard synthetic immunosuppressive drugs and in some cases other biologic agents; Written informed consent form approved for each hospital was requested and obtained from each patient prior to the onset of etoposide treatment.;Inclusion criteria: AOSD was diagnosed according to the criteria described by Yamaguchi et al; All patients had previously received standard synthetic immunosuppressive drugs and in some cases other biologic agents; Written informed consent form approved for each hospital was requested and obtained from each patient prior to the onset of etoposide treatment.;Inclusion criteria: AOSD was diagnosed according to the criteria described by Yamaguchi et al; All patients had previously received standard synthetic immunosuppressive drugs and in some cases other biologic agents; Written informed consent form approved for each hospital was requested and obtained from each patient prior to the onset of etoposide treatment.;Inclusion criteria: AOSD was diagnosed according to the criteria described by Yamaguchi et al; All patients had previously received standard synthetic immunosuppressive drugs and in some cases other biologic agents; Written informed consent form approved for each hospital was requested and obtained from each patient prior to the onset of etoposide treatment.

Exclusion criteria

Exclusion criteria: Before the initiation of etoposide treatment, the presence of infections, including hepatitis B or hepatitis C virus infections; MAS was defined following the diagnostic criteria proposed by the updated in 2004 and by Fardet L. et al. were excluded;Exclusion criteria: Before the initiation of etoposide treatment, the presence of infections, including hepatitis B or hepatitis C virus infections; MAS was defined following the diagnostic criteria proposed by the updated in 2004 and by Fardet L. et al. were excluded;Exclusion criteria: Before the initiation of etoposide treatment, the presence of infections, including hepatitis B or hepatitis C virus infections; MAS was defined following the diagnostic criteria proposed by the updated in 2004 and by Fardet L. et al. were excluded;Exclusion criteria: Before the initiation of etoposide treatment, the presence of infections, including hepatitis B or hepatitis C virus infections; MAS was defined following the diagnostic criteria proposed by the updated in 2004 and by Fardet L. et al. were excluded;Exclusion criteria: Before the initiation of etoposide treatment, the presence of infections, including hepatitis B or hepatitis C virus infections; MAS was defined following the diagnostic criteria proposed by the updated in 2004 and by Fardet L. et al. were excluded

Design outcomes

Primary

MeasureTime frame
percentage of patients with the Pouchot score dropped by more than two points;

Secondary

MeasureTime frame
Improvement of laboratory indicators and clinical indicators;

Countries

China

Contacts

Public ContactWang Xiaodong;Wang Xiaodong;Wang Xiaodong;Wang Xiaodong;Wang Xiaodong ;;;;

Department of Rheumatology, Renji Hospital South Campus, School of Medicine, Shanghai JiaoTong University;Department of Rheumatology, Renji Hospital South Campus, School of Medicine, Shanghai JiaoTong University;Department of Rheumatology, Renji Hospital South Campus, School of Medicine, Shanghai JiaoTong University;Department of Rheumatology, Renji Hospital South Campus, School of Medicine, Shanghai JiaoTong University;Department of Rheumatology, Renji Hospital South Campus, School of Medicine,

wht880609@126.com;wht880609@126.com;wht880609@126.com;wht880609@126.com;wht880609@126.com+86 13661926959;+86 13661926959;+86 13661926959;+86 13661926959;+86 13661926959

Outcome results

None listed

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