The purpose of this study is to evaluate the efficiency and safety of weekly Cisplatin
/Liposome paclitaxel concurrent chemoradiothrapy in the treatment of locally advanced
cervical cancer in elderly women.
Drug: liposome paclitaxel
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Full eligibility criteria for NCT01594099
Ages eligible for Study
65 Years to 80 Years
Genders eligible for Study
Accepts Healthy Volunteers
Histologically proven squamous carcinoma of cervix
FIGO stageⅡB and ⅢB
Over 65 years
Do not receive other treatment
Performance index ECOG grade 0 to 2
Normal hematological parameters
Normal renal and liver function tests
Concomitant disease which may adversely affect the outcome
Poor nutritional status
Medical or psychological condition precluding treatment
Concurrent treatment for any cancer
All locations for NCT01594099
View full eligibility
Tris trial is registered with FDA with number: NCT01594099. The sponsor of the trial is Health Science Center of Xi’an Jiaotong University and it is looking for 45 volunteers for the current phase.
Official trial title: Weekly Cisplatin or Weekly Liposome Paclitaxel Concurrent Radiation Therapy in Treating Elderly People With Cervical Cancer
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