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Spots Global Cancer Trial Database for Clinical Study in Post-operation Treatment of Cervical Cancer

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Clinical Study in Post-operation Treatment of Cervical Cancer

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

Study ID: NCT01418859

Conditions

Cervical Cancer

Interventions

Study Description

Brief 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.

Eligibility

Minimum Age: 20 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Xi'an Jiaotong University College of Medicine, Xi'an, Shanxi, China

Contact Details

Name: Chen M W, M.D

Affiliation: Affiliated Hospital of Medical College of Xo'an Jiaotong University

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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