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Efficacy and safety of cyclosporine and azathioprine in patients with refractory ITP

Efficacy and safety of cyclosporine and azathioprine in patients with refractory ITP

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900027753
Enrollment
Unknown
Registered
2019-11-25
Start date
2019-12-01
Completion date
Unknown
Last updated
2019-12-10

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

Conditions

Primary Immune Thrombocytopenia

Interventions

Group 1:Using cyclosporine A for treatment
Group 2:Using azathioprine for treatment
Control group:Treatment with glucocorticoids

Sponsors

the Second Affiliated Hospital of Kunming Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-75, male and female; 2. It meets the following diagnostic criteria for ITP (according to the 2016 version of Chinese expert consensus on diagnosis and treatment of adult primary immune thrombocytopenia): 2 or more laboratory blood routine examinations showed decreased platelet count and no abnormal blood cell morphology; 3. Spleen generally not enlarged; 4. The number of megakaryocytes in bone marrow examination was increased or normal, and there was maturation disorder; 5. Platelet count =30x10^9/L but bleeding; 6. Patients who had been treated with glucocorticoid but had poor efficacy or had contraindications for adrenocorticoid use; 7. Patients with ITP who failed splenectomy; 8. ITP patients who failed to respond to other second-line drugs;Voluntary hospitalization and informed consent.

Exclusion criteria

Exclusion criteria: 1. Received chemotherapy, anticoagulant drugs or other treatments that might affect platelet count in the first 3 weeks of the study; 2. Serious heart, lung, liver, renal insufficiency diseases; 3. Severe immunodeficiency, or systemic autoimmune disease; 4. Patients with severe hypertension; 5. The investigator considers it inappropriate to participate in any other condition of this trial; 6. All kinds of congenital thrombocytopenia, pseudothrombocytopenia and other secondary thrombocytopenia.

Design outcomes

Primary

MeasureTime frame
platelets counts;

Countries

China

Contacts

Public ContactZeping Zhou

The Second Affiliated Hospital of Kunming Medical University

zhouzeping@outlook.com+86 18788571605

Outcome results

None listed

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