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 Trial Title: 
 Clinical Study in Post-operation Treatment of Cervical Cancer 
 NCT ID: 
 NCT01418859 
 Condition: 
 Cervical Cancer 
 Conditions: Official terms: 
 Uterine Cervical Neoplasms 
 Conditions: Keywords: 
 cervical cancer 
 postoperation 
 chemotherapy 
 radiotherapy 
 Study type: 
 Observational 
 Overall status: 
 Unknown status 
 Study design: 
 Time perspective: 
 Prospective 
 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. 
 Criteria for eligibility: 
 Study pop: 
  
 patients who underwent the cervical cancer radical surgery in three months have higt risk
factors which including deep stromal invasion,large primary tumour and/or lymphovascular
spase invasion. 
  
 Sampling method: 
 Probability Sample 
 Criteria: 
  
 Inclusion Criteria:
  1. patients who underwent the cervical cancer radical surgery in three months have higt
     risk factors which including deep stromal invasion,large primary tumour and/or
     lymphovascular spase invasion;
  2. squamous carcinoma;
  3. age<70;
  4. Gynecologic Oncology Group (GOG):0-2.
Exclusion Criteria:
  1. negative nodes,surgical margin,and/or parametrium;
  2. No serious damage to the liver and kidney function, no hypertension,diabetes and
     other effects of therapy complications. 
  
 Gender: 
 Female 
 Minimum age: 
 20 Years 
 Maximum age: 
 70 Years 
 Healthy volunteers: 
 No 
 Locations: 
 Facility: 
  
 Name: 
 Xi'an Jiaotong University College of Medicine 
 Address: 
  
 City: 
 Xi'an 
 Zip: 
 710061 
 Country: 
 China 
 Status: 
 Recruiting 
 Contact: 
  
 Last name: 
 Zi Liu, M.D 
 Phone: 
 086-18991232167 
 Email: 
 18991232167@189.cn 
 Contact backup: 
  
 Last name: 
 Tao Wang, M.D 
 Phone: 
 086-18991232386 
 Email: 
 18991232386@189.cn 
 Investigator: 
  
 Last name: 
 Tao Wang, M.D 
 Email: 
 Sub-Investigator 
 Start date: 
 August 2011 
 Completion date: 
 December 2015 
 Lead sponsor: 
  
 Agency: 
 Health Science Center of Xi'an Jiaotong University 
 Agency class: 
 Other 
 Source: 
 Health Science Center of Xi'an Jiaotong University 
 Record processing date: 
 ClinicalTrials.gov processed this data on November 12, 2024 
 Source: ClinicalTrials.gov page: 
 https://clinicaltrials.gov/ct2/show/NCT01418859