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A randomized controlled trail of bone marrow sparing intensity modulated radiotherapy in patients with cervical cancer

A randomized controlled trail of bone marrow sparing intensity modulated radiotherapy in patients with cervical cancer

Status
Active, not recruiting
Phases
Phase 3
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000035448
Enrollment
Unknown
Registered
2020-08-11
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

Cervical cancer

Interventions

Experimental group:bone marrow sparing intensity modulated radiotherapy

Sponsors

Shanghai Jiao Tong University Affliated Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Cervical cancer patients diagnosed by pathology for the first time; 2. According to the 2014 FIGO cervical cancer staging for patients with stage IB-IVa; 3. Aged from 18 to 70 years old; 4. ECOG general condition score 0-2, weight loss less than 10% within 6 months, can tolerate radiotherapy and chemotherapy; 5. No other second primary cancer within 5 years; 6. It is confirmed that there is no distant metastasis by MRI or CT, chest X-ray, B-ultrasound, etc.; 7. No other serious medical complications such as coronary heart disease, hypertension, tuberculosis, etc.; 8. Non-pregnancy and lactation period; 9. Those who are expected to survive more than 12 months; 10. Laboratory examination before radiotherapy and chemotherapy meets the following conditions: blood function: absolute neutrophil count (ANC) >=2x10^9/L, platelet count >=100x10^9/L and hemoglobin >=9g/dL; 11. The subject agrees and signs the informed consent form (if the subject is not capable of judgment, his legal guardian is required to sign the informed consent form).

Exclusion criteria

Exclusion criteria: 1) Accompanied by other malignant tumors, including malignant tumors discovered at the same time and in the past; 2) Combined with hematological diseases; 3) Past medical history of pelvic radiotherapy; 4) Patients with severe liver, kidney and nervous system diseases and mental illness; 5) Circumstances where other examiners believe that there are sufficient reasons to be unqualified from the registration study: if there is a potential inconsistency with the clinical plan, etc.; 6) Unable or unwilling to sign informed consent

Design outcomes

Primary

MeasureTime frame
Blood routine;

Secondary

MeasureTime frame
Local recurrence;

Countries

China

Contacts

Public ContactXiaojing Yang

Department of Radiation Oncology, Shanghai Jiao Tong University Affliated Sixth People's Hospital

yangxj717@163.com+86 21 24058972

Outcome results

None listed

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