Skip to content

99Tcm-Sulfur Colloid SPECT/CT defined active Bone Marrow Protection combined with Pegylated Recombinant Human Granulocyte Colony-Stimulating Factor Protection for the prevention of Severe neutropenia induced by concurrent chemoradiotherapy in locally advanced cervical cancer

99Tcm-Sulfur Colloid SPECT/CT defined active Bone Marrow Protection combined with Pegylated Recombinant Human Granulocyte Colony-Stimulating Factor Protection for the prevention of Severe neutropenia induced by concurrent chemoradiotherapy in locally advanced cervical cancer

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087321
Enrollment
Unknown
Registered
2024-07-25
Start date
2024-07-31
Completion date
Unknown
Last updated
2024-07-29

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:Pegylated Recombinant Human Granulocyte Colony-Stimulating Factor in combination with Active Bone Marrow Protection
Control group:Active Bone Marrow Protection

Sponsors

The Second People's Hospital of Yibin City
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 70 years old; 2. Pathologically confirmed cervical cancer,FIGO staging locally advanced cervical cancer (1B2/2A2/2B and above); 3. ECOG performance status 0 - 1; 4. More than the expected survival time in One year; 5. WBC=4×10^9/L, ANC=2×10^9/L Hemoglobin=110g/L, Platelets =100×10^9/L; Bilirubin <=2*ULN; ALT and AST <=2.5*ULN; BUN <=1.5*ULN; Creatinine<=1.5*ULN; 6. Signed study-specific informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients currently or previously receiving systemic chemotherapy or pelvic radiotherapy. 2. Patients with any confirmed diseases causing peripheral blood cell abnormalities. 3. Patients with active infectious diseases. 4. Patients with a history of mental illness. 5. Patients with a history of severe cardiovascular and cerebrovascular diseases, HIV, etc. 6. Pregnant and lactating women. 7. Patients with tumor invasion of the bladder and rectum, assessed by the study to be at risk of perforation. 8. Patients deemed unsuitable for participation in this study by the investigators.

Design outcomes

Primary

MeasureTime frame
Neutropenia;

Secondary

MeasureTime frame
Leukopenia;Anemia;Thrombocytopenia;Duration of Severe Neutropenia;Number of Delays or Interruptions in Chemotherapy Cycles;Incidence of Febrile Neutropenia;Quality of Life;

Countries

China

Contacts

Public ContactShanbing Wang

The Second People's Hospital of Yibin City

275915691@qq.com+86 136 5903 7910

Outcome results

None listed

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