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A Real-World Study of Yisui Shengxue Pills for the Treatment of Chemoradiotherapy-Related Myelosuppression

A real-world study on Yisui Shengxue Wan for chemoradiotherapy-related myelosuppression.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001966
Enrollment
Unknown
Registered
2025-10-22
Start date
2026-01-01
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Bone marrow suppression after chemoradiotherapy

Interventions

Observation Group:In addition to standard treatment, the in-hospital preparation "Yisui Shengxue Pills" from Gansu Province was used (8 pills three times a day, orally).
Control Group:According to the guidelines, standardized radiotherapy and chemotherapy, as well as conventional Western medical supportive treatment for myelosuppression, have been completed.

Sponsors

Gansu Provincial Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Voluntary participation and written informed consent; 2. Age 18-80 years, regardless of gender; 3. Patients with a confirmed diagnosis of malignant tumor by histopathology or cytology; 4. Normal blood count, liver and kidney function, and electrocardiogram before radiotherapy/chemotherapy, with no symptoms of infection or fever; 5. Patients with indications for radiotherapy/chemotherapy and intended treatment; 6. Patients with no major organ damage and an estimated survival time of more than 3 months; 7. Patients with a KPS score = 70.

Exclusion criteria

Exclusion criteria: 1. Patients with underlying lung inflammation, or serious heart, liver, or kidney diseases, or those with severe infections; 2. Patients with mental illness or a history of severe mental illness; 3. Patients with myelodysplastic syndrome or primary hematologic disease; 4. Patients who have previously received other treatments similar to those in this study that may affect the observed outcomes; 5. Pregnant or breastfeeding women, or women who refuse contraception during the treatment observation period; 6. Patients with a history of severe allergies or specific physical conditions; 7. Patients with drug abuse or alcohol addiction; 8. Patients currently participating in other clinical trials; 9. Patients with allergies to the main ingredients of the investigational drug.

Design outcomes

Primary

MeasureTime frame
Blood Routine;

Secondary

MeasureTime frame
Erythropoietin;Thrombopoietin;Granulocyte colony-stimulating factor;

Countries

China

Contacts

Public ContactHongtao Luo

Gansu Provincial Hospital of Traditional Chinese Medicine

hongtaoluo@126.com13919345474

Outcome results

None listed

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