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A clinical study of romiplostim in the treatment of refractory/relapsed immune thrombocytopenia

A clinical study of romiplostim in the treatment of refractory/relapsed immune thrombocytopenia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500097340
Enrollment
Unknown
Registered
2025-02-18
Start date
2025-01-23
Completion date
Unknown
Last updated
2025-02-24

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

Conditions

immune thrombocytopenia

Interventions

Divided by disease course into New diagnosed ITP, chronic ITP, persistent ITP:NA

Sponsors

The affiliated people's hospital of Ningbo University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. According to the "Chinese Guidelines for Diagnosis and Treatment of Adult Primary Immune Thrombocytopenia (2020 Edition)", patients diagnosed with ITP who are ineffective in splenectomy or have not undergone splenectomy but are ineffective in treating = 2 types of ITP, or who relapse after ITP treatment. 2. Platelet count<30 × 10^9/L before using romiplostim; 3. ECOG score = 2 points; 4. Complete clinical data and voluntary signing of informed consent form.

Exclusion criteria

Exclusion criteria: 1. Merge other blood system diseases; 2. Merge important organ dysfunction; 3. Merge uncontrollable infections, such as active tuberculosis, etc; 4. Recent occurrence of any arterial or venous thrombosis, or clinical symptoms and medical history indicating thrombophilia; 5. Pregnant or lactating women; 6. Allergic to romiplostim.

Design outcomes

Primary

MeasureTime frame
platelet count;

Secondary

MeasureTime frame
Liver function;

Countries

China

Contacts

Public ContactShen Minli

The affiliated people's hospital of Ningbo University

347413609@qq.com+86 15857342004

Outcome results

None listed

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