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Effect of pricking and cupping on chemotherapy-induced thrombocytopenia: a multicenter randomized controlled trial

Clinical study for chemotherapy-induced thrombocytopenia treated by pricking and cupping

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021664
Enrollment
Unknown
Registered
2019-03-04
Start date
2019-03-05
Completion date
Unknown
Last updated
2019-10-14

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

Conditions

Chemotherapy-induced thrombocytopenia

Interventions

Experimental group:pricking and cupping
Control group:Basic treatment

Sponsors

The Third Hospital Affiliated to Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. All cases were diagnosed by histopathology or cytopathology, in line with the "Malignant tumor diagnosis and efficacy criteria" without chemotherapy relative contraindications; and in line with the diagnostic criteria for tumor chemotherapy-induced thrombocytopenia; 2. Patients who receive chemotherapy with gemcitabine or a platinum-containing regimen; 3. Aged between 18-80 years old male and female; 4. The physical condition of the subject is acceptable, Karnofsky > 70 points; 5. The estimated survival time is = 3 months; 6. There is no serious damage to vital organs such as heart, liver, spleen, lung, kidney and bone marrow; 7. No coagulopathy 8. No treatment with rhTPO, rhIL-11, etc. one month before chemotherapy; 9. Platelet count was normal before chemotherapy, platelet (50~75)×10^9/L with or without leukocytes, granulocytes and hemoglobin decreased during chemotherapy; 10. No previous history of drug and food allergies; 11. Subject compliance, agree and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Thrombocytopenia caused by other causes; 2. Pregnancy or intentional pregnancy or lactation women; 3. Those with severe cognitive impairment and mental illness; 4. Consolidation of seriously infected persons; 5. Those with combined blood system diseases and splenomegaly; 6. Secondary liver, spleen and bone metastases; 7. Those who have undergone radiotherapy before treatment; 8. A history of thrombosis in the first three months of treatment.

Design outcomes

Primary

MeasureTime frame
Platelet count;

Secondary

MeasureTime frame
The time when platelets return to normal;Recurrence rate of thrombocytopenia;Coagulation function;Quality of life;

Countries

China

Contacts

Public ContactJinchang Huang

The Third Hospital Affiliated to Beijing University of Chinese Medicine

zryhhuang@163.com+86 13910801918

Outcome results

None listed

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