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An registration study for safety profile of Total glucosides of paeony in patients with juvenile idiopathic arthritis(JIA)

An registration study for safety profile of Total glucosides of paeony in patients with juvenile idiopathic arthritis(JIA)

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400086701
Enrollment
Unknown
Registered
2024-07-09
Start date
2024-08-01
Completion date
Unknown
Last updated
2024-07-15

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

Conditions

Juvenile idiopathic arthritis

Interventions

Case series:Total glucosides of paeony (TGP) capsules

Sponsors

Department of Rheumatology and Immunology, Beijing Chilren's Hospital,Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: (1) Patient's age is less than 18 years old. (2) Patients diagnosed with JIA in the Department of Rheumatology and regularly followed up. (3) Patients who have received total glycosides of peony monotherapy/combination therapy for the first time. (4) Background medications may include one oral NSAIDs, as well as no more than three combination immunosuppressants (methotrexate, leflunomide, hydroxychloroquine, sulfasalazine, cyclosporine, thalidomide, and mycophenolate), steroids, biologics, and tofacitinib. Note: Patients are those who have taken total glycosides of peony for the first time since the start of this study or have previously taken it, but have not taken it within 3 months of the screening period.

Exclusion criteria

Exclusion criteria: (1) Patients who are unable to sign a written informed consent form. (2) Patients who are allergic to research drugs. (3) Patients have advanced, severe, or life-threatening illnesses, any medical or mental conditions. (4) Other reasons have been determined by the researcher to be unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
The incidence of adverse events/reactions during the 8-week medication period.;

Countries

China

Contacts

Public ContactLI CAIFENG

Beijing Chilren's Hospital,Capital Medical University

caifeng_li@yeah.net+86 139 1042 2991

Outcome results

None listed

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