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Efficacy and safety of PBMS-RT(Pelvic Bone Marrow Sparing Radiotherapy) compared with conventional radiotherapy in patients with cervical cancer

Efficacy and safety of PBMS-RT(Pelvic Bone Marrow Sparing Radiotherapy) compared with conventional radiotherapy in patients with cervical cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600131480
Enrollment
Unknown
Registered
2026-09-02
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-09-07

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

Conditions

Cervical cancer

Interventions

PBMS Group:Pelvic Bone Marrow Sparing Radiotherapy

Sponsors

The First Affiliated Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Confirmed by pathological gynecologic examination as cervical cancer; 2. Inclusion of patients with stage Ib2-IIIb cervical cancer without prior radiation or chemotherapy (staging according to the 2018 NCCN guidelines FIGO staging); 3. Patient age >= 20 years and <= 80 years; 4. Patient voluntarily participates and signs an informed consent form, has good compliance, and can cooperate with the study according to the protocol requirements.

Exclusion criteria

Exclusion criteria: 1. Cases requiring abdominal extended-field irradiation. 2. History of prior bone-related diseases (e.g., femoral head necrosis) or muscle-related diseases, or prior hip joint implantation or femoral head replacement. 3. History of prior bisphosphonate therapy, hormone replacement therapy, or similar treatments. 4. History of occupational exposure factors (e.g., paint, decoration, nail art industries) and blood-related diseases. 5. History of prior pelvic irradiation. 6. Planned participation in other clinical studies. 7. Other conditions judged by the investigator that may affect the conduct of the clinical study or the interpretation of the study results. 8. Refusal or inability to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
Local Control Rate;

Secondary

MeasureTime frame
Hematotoxicity;Intestinal injury;Urinary system injury;Skeletal injury;

Countries

China

Contacts

Public ContactLi Guang

The First Affiliated Hospital of China Medical University

lg13804058616@163.com+86 138 0405 8616

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Sep 19, 2026