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The research scheme of TCM syndromic characteristics of cervical cancer and the key role targets and curative effect observation of traditional Chinese medicine combined with radiotherapy and chemotherapy

The research scheme of TCM syndromic characteristics of cervical cancer and the key role targets and curative effect observation of traditional Chinese medicine combined with radiotherapy and chemotherapy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066917
Enrollment
Unknown
Registered
2022-12-21
Start date
2022-12-31
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

cervical carcinoma

Interventions

Intervention group:Radiochemotherapy+Zhenqi Liujun Anti cancer Granule
Control group:Radiochemotherapy

Sponsors

The Traditional Chinese Medicine Hospital Affiliated to Southwest
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: ? Cervical cancer definitely diagnosed by histology or pathology? Subjects did not receive any systematic anti-tumor treatment, such as chemotherapy, radiotherapy, immunotherapy, biological or hormone therapy, and did not receive any VEGFR inhibitor treatment in the past three months;? There was no operation or large biopsy within 4 weeks after randomization;? Age = 18 years and = 75 years, weight = 40Kg;? The subjects had no dysfunction of heart, liver, kidney and hematopoietic system; The definition is as follows: absolute neutrophil count (ANC)>1.5 × 109/L,; Platelets>100 × 109/L; Hemoglobin = 90g/L; Total bilirubin = 1.5 × Upper limit of normal (ULN); AST(SGOT)/ALT(SGPT)=2.5 × The upper limit of normality, if it is clearly attributable to liver metastasis, is less than 5 times the upper limit of normality; UPCR<1.0;? Physical condition score: ECOG 0~2, KPS = 50;? Estimated survival time = 12 weeks;? Fully understand the study and voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Prepare for tumor immunotherapy;2. Patients with unstable brain metastasis;3. Pregnant and lactating women and patients of childbearing age who are unwilling to take contraceptive measures;4. Patients with mental illness or mental retardation;5. Known to be severely intolerant of the study drug;6. Patients with serious diseases such as heart, liver, kidney and hematopoietic system (1. Absolute neutrophil count (ANC) 1.5 × Upper limit of normal (ULN); AST(SGOT)/ALT(SGPT)>2.5 × Normal upper limit, if it is clearly attributable to liver metastasis, = 5 times of normal upper limit; 3. Creatinine clearance rate 160mmHg or diastolic blood pressure>100mmHg after single drug treatment), severe arrhythmia, and cardiac function class III-IV (NYHA classification).

Design outcomes

Primary

MeasureTime frame
Occurrence rate of radioactive inflammation;Degree of bone marrow suppression;T lymphocytes;

Secondary

MeasureTime frame
Quality of life;Adverse events;

Countries

China

Contacts

Public ContactZhongming Yang

The Traditional Chinese Medicine Hospital Affiliated to Southwest

yzm265@163.com13438010665

Outcome results

None listed

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