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Clinical study of immune thrombocytopenia with syndrome of qi failing to keep blood

Clinical study of immune thrombocytopenia with syndrome of qi failing to keep blood

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17014236
Enrollment
Unknown
Registered
2017-12-31
Start date
2015-12-01
Completion date
Unknown
Last updated
2018-01-08

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

Conditions

Immune thrombocytopenia

Interventions

Group 1:Siwu Ejiao Decoction
Group 1:Sijunzi decoction plus Siwu Ejiao Decoction

Sponsors

Xiyuan Hospital, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Meet the ITP diagnostic criteria, duration = 3 months; 2. The average platelet count =10×10^9/L in 2 weeks; 3. aged between 18 to 75 years old male and female; 4. did not participate in other clinical studies, voluntary in this study.

Exclusion criteria

Exclusion criteria: 1. Severe gastrointestinal bleeding (poor control), or (and) organ bleeding; 2. More than 2 subcutaneous mucosal bleeding or ecchymosis; 3. Subjects used other drugs other than ITP, such as IVIG, CTX, VCR, rTPO, IL-11, rituximab and elquipep, within 14 days before entering the trial. 4. does not meet the criteria for inclusion in clinical research programs; 5. organ insufficiency: serum creatinine greater than the upper limit of normal; alanine aminotransferase, aspartate transaminase, bilirubin greater than 2 times the upper limit of normal; NYHA classification = ? level; 6. Pregnancy, lactating women, allergies; 7. To participate in other clinical studies.

Design outcomes

Primary

MeasureTime frame
immune cells: CD4+ CD25+ CD127low T cells; CD19+ CD24+ CD27+ (or CD19+ CD24+ CD38hi); CD19 + IL-10+; Th17: CD4+ CD17+ IFN; Th1, Th2;

Contacts

Public ContactHu Xiaomei

Xiyuan Hospital, China Academy of Chinese Medical Sciences

huxiaomei_2@163.com+86 18610350593

Outcome results

None listed

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