Skip to content

A multicenter, randomized controlled trial comparing Shengbaikeli with Diyushengbai Tablets for the treatment of leukopenia and alleviation of cancer-related fatigue

A multicenter, randomized controlled trial comparing Shengbaikeli with Diyushengbai Tablets for the treatment of leukopenia and alleviation of cancer-related fatigue

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123973
Enrollment
Unknown
Registered
2026-05-06
Start date
2026-05-12
Completion date
Unknown
Last updated
2026-05-11

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

Conditions

malignant tumors

Interventions

Diyushengbai group:Diyushengbai
Shengbaikeli group:Shengbaikeli

Sponsors

The First People’s Hospital of Lianyungang
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with solid tumors or hematologic tumors confirmed by histopathology or cytology; 2. Aged 18-80 years, any gender; 3. Developed grade I-II leukopenia (2.0 x 10^9/L = 3 months; 6. Voluntarily participate and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Individuals known to be allergic to Granule for Increasing White Blood Cells, Diyu Shengbai Tablets, or any of their ingredients. 2. Those with yin deficiency with excessive fire, a tendency to bleed, and pregnant women. 3. Those with severe heart, liver, or kidney dysfunction (e.g., NYHA heart function class III-IV, ALT/AST > 3 times the upper limit of normal, Cr > 2 times the upper limit of normal). 4. Those with active infections or uncontrolled serious comorbidities; those with hematopoietic dysfunction. 5. During the study, those planning to use or who have already used granulocyte colony-stimulating factors (G-CSF/GM-CSF), other Chinese or Western medicines for increasing white blood cells (except the study drug). Chinese tonic preparations such as: Shenqi Fuzheng Injection, Zhenqi Fuzheng Granules, Fuzheng Capsules, etc.

Design outcomes

Primary

MeasureTime frame
Blood routine ;

Secondary

MeasureTime frame
Quality of life score;

Countries

China

Contacts

Public ContactXiaodong Jiang

The First People’s Hospital of Lianyungang

jxdysy1970@163.com+86 189 6132 6201

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026