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Clinical Research on Radiotherapy at Diferrent Time for Unresectable Cervical Cancer

Clinical Research on Radiotherapy at Diferrent Time for Unresectable Cervical Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-10001228
Enrollment
Unknown
Registered
2010-09-28
Start date
2009-11-02
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Cervical Cancer

Interventions

Morning-irradiated group:Irradiated at 9:00-11:00. External radiation: 6-MV X ray, whole pelvic DT30-40GY/15-20F, four-field DT10-20GY/5-10F, 2GY/F. After-loading therapy: DT42GY/7-8F, 5-6 GY/F.
Evening-irradiated group:Irradiated at 21:00-23:00. External radiation: 6-MV X ray, whole pelvic DT30-40GY/15-20F, four-field DT10-20GY/5-10F, 2GY/F. After-loading therapy: DT42GY/7-8F, 5-6 GY/F.

Sponsors

Tumor Hospital of Yunnan Province (The Third Affliated Hospital of Kunming Medical College)
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Female aged 18 to 65 years old; 2. Able and willing to provide signed informed consent; 3. Patients with clinical stage IIb-IVa cervical carcinoma; 4. Patients had an ECOG performance status 0 to 2; 5. Cervical carcinoma without distant metastasis; 6. Patients have never received pelvic cavity radiotherapy and haven't receive systemic chemotherapy in 4 weeks before; 7. Pregnancy test results are negative; 8. Normal bone marrow hemopoiesis; 9. Normal hepatic and renal function; 10. Patients without important systems dysfunction and serious malnutrition.

Exclusion criteria

Exclusion criteria: 1. Patients have other carcinoma in situ; 2. Contraindication to radiotherapy on other organs; 3. Patients who is participating or planning to participate in other clinical trial.

Design outcomes

Primary

MeasureTime frame
Cell cycle;Circadian gene expression;DNA damages;Cell apotosis;Short-term effect;Acute radiation damage;

Secondary

MeasureTime frame
Survival rate;Tumor markers;Micronucleated cell;Biochemistry exmamination;Late complication;GSH concentration;Median survival time (MST);Blood routine test;HPV DNA;

Countries

China

Contacts

Public ContactWenhui Li
wenhuili64@yahoo.com.cn+86 13888087323

Outcome results

None listed

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