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Construction and Empirical Study of a Comprehensive Prevention and Control Model Involving Clinical Pharmacist Intervention for Chemotherapy-Induced Myelosuppression

Construction and Empirical Study of a Comprehensive Prevention and Control Model Involving Clinical Pharmacist Intervention for Chemotherapy-Induced Myelosuppression

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122426
Enrollment
Unknown
Registered
2026-04-14
Start date
2026-04-15
Completion date
Unknown
Last updated
2026-04-20

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

Conditions

Chemotherapy-induced myelosuppression

Interventions

Control group:Treated in accordance with normal medical procedures
Intervention group:Risk assessment of bone marrow suppression, medication recommendations, intervention for adverse reactions, drug adjustment, treatment evaluation, patient education, etc.

Sponsors

Yuebei People’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18 - 75 years old; 2. Patients diagnosed with malignant solid tumors at stage III-IV by histopathological examination (priority will be given to tumor types with high risk of bone marrow suppression such as lung cancer and breast cancer); 3. Undergoing bone marrow suppressive chemotherapy (including platinum-based/anthracycline-based/paclitaxel-based drugs), with an expected survival period of more than 6 months; 4. Having experienced grade II or above bone marrow suppression in previous chemotherapy (according to CTCAE v6.0) or the current treatment plan is expected to carry a medium to high risk of suppression; 5. Have signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Previously had hematopoietic system diseases such as myelodysplastic syndrome, aplastic anemia, leukemia, etc.; 2. Patients allergic to G-CSF, TPO/TPO-RA or tralaxel; 3. Patients with tuberculosis, HIV positive, uncontrolled heart failure, renal failure or liver failure (Child-Pugh C grade) during the study period; 4. Patients with mental disorders, cognitive deficits or unable to complete follow-up; 5. Patients with concurrent radiotherapy plan during the study period.

Design outcomes

Primary

MeasureTime frame
Incidence of grade III/IV bone marrow suppression;Duration of bone marrow suppression;

Secondary

MeasureTime frame
The rate of adjusting chemotherapy drug dosage;The usage rate of G-CSF/TPO/TPO-RA;Complication occurrence rate;Hospitalization period;Medical expenses;Patient quality of life assessment;

Countries

China

Contacts

Public ContactHaiying Zhong

Yuebei People’s Hospital

cpuzhy123@163.com+86 751 691 3465

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 23, 2026