Clinical Trials Directory

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UnknownNCT01418859

Clinical Study in Post-operation Treatment of Cervical Cancer

Status and the Application of Topotecan at Post-operation Treatment of Cervical Cancer

Status
Unknown
Phase
Study type
Observational
Enrollment
183 (estimated)
Sponsor
Xi'an Jiaotong University · Academic / Other
Sex
Female
Age
20 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The purpose of the research is to evaluate the effect of additional chemotherapy in postoperation therapy of cervical cancer patients with risk factors (big tumor, deep invasion or tumor thrombi in the vascular system).

Detailed description

Cervical cancer has a very high morbidity. Many patients need additional therapy after surgery in order to elevate the survival rate and life quality. In this research, we are going to give additional therapy to patients who have big tumor, deep invasion or tumor thrombi in the vascular system after surgery. randomized control method will be used in this research, in order to compare the survival rate and side effects between radiation therapy only, concurrent chemoradiotherapy, and concurrent chemoradiotherapy with additional chemotherapy. 3D-CRT and Topotecan will be used in this research.

Conditions

Timeline

Start date
2011-08-01
Primary completion
2012-12-01
Completion
2015-12-01
First posted
2011-08-17
Last updated
2012-03-21

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT01418859. Inclusion in this directory is not an endorsement.