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Prospective clinical study for molecular typing of locally advanced cervical cancer

Prospective clinical study for molecular typing of locally advanced cervical cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900021605
Enrollment
Unknown
Registered
2019-03-01
Start date
2019-05-01
Completion date
Unknown
Last updated
2019-03-04

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

Conditions

Cervical cancer

Interventions

Sponsors

Zhujiang Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Female aged 18 to 75 years; 2. Local advanced cervical cancer patients diagnosed by pathology and FIGO stages; 3. ECOG PS 0-1; 4. At least one CR/MRI lesion can be measured; 5. Life expectancy = 3 months; 6. Peripheral blood images, liver and kidney functions are within the following permitted limits (tested within 7 days before the treatment); - Leukocyte(WBC) = 3.0×10^9/L or Neutrophil(ANC) = 1.5×10^9/L; - Hemoglobin (HGB) = 80g/L; - Platelet(PLT) = 100×10^9/L; - Liver transaminase (AST and ALT) < 3.0×ULN; - Total bilirubin(TBIL) < 1.5×ULN; - CREAT < 1.5×ULN. 7. Patients of child-bearing age must take effective birth control measures; 8. Sign the informed consent. Those who meet all of the criteria above will be included in the study.

Exclusion criteria

Exclusion criteria: 1. Have a history of other malignant tumors in the past 5 years, except for the cured basal cell carcinoma of the skin and carcinoma in situ of the cervix; 2. Those who are known to be allergic to the drug ingredients involved in the study; 3. Patients with a history of severe allergies or allergic constitution; 4. Pregnant or lactating women; 5. Patients with drug addiction, substance abuse, long-term alcohol abuse and AIDS; 6. Patients with cardiac failure or arrhythmia; Those who meet any of the criteria above will not be included in the study.

Design outcomes

Primary

MeasureTime frame
OS;

Secondary

MeasureTime frame
ORR;PFS;QOL;

Countries

China

Contacts

Public ContactJian Zhang

Zhujiang Hospital of Southern Medical University

blacktiger@139.com+86 13925091863

Outcome results

None listed

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