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临床试验/CTRI/2009/091/000137
CTRI/2009/091/000137进行中(未招募)4 期

Effectiveness and safety of 2 versus 3 doses of HPV Vaccine in preventing cervical cancer: An Indian multi-centre randomized trial.

WHO0 个研究点目标入组 20,000 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
进行中(未招募)
发起方
入组人数
20,000

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Inclusion exclusion criteria:Healthy, ambulant, unmarried girls aged 10-18 years with intact uterus, residing in the selected villagesEligible girl as well as either or both the parents/legal guardian willing to sign a written informed consentExclusion criteria:·

排除标准

  • Inclusion exclusion criteria:Healthy, ambulant, unmarried girls aged 10-18 years with intact uterus, residing in the selected villagesEligible girl as well as either or both the parents/legal guardian willing to sign a written informed consent·Participant having any allergies to medications, food, or any vaccine·Participant who has experienced a serious reaction after receiving any vaccination·Participant having any health problem with asthma, heart disease, lung disease, kidney disease, metabolic disease (e.g., diabetes), epilepsy or any neurological illness, mental or physical disability or blood dyscrasia·Participant who has/had cancer, leukemia, AIDS, or any other immune system problem·Participant who has taken cortisone, prednisone, other steroids, or anticancer drugs, or had radiation treatments in the past 3 months·Participant having any prior history of genital warts or treatment for genital warts·Participant who has received a blood transfusion, any blood products, or been given a medicine called immune (gamma) globulin in the past year·Participant has undergone any surgical procedure for the removal of the uterus·Participant married or engaged to be married in the next 6 months·Participant not willing to use any effective contraception through month 7 of the study if she gets married ·Participant has any plans to permanently relocate from the area prior to the completion of the study or to leave for an extended period of time when study visits would need to be scheduled?.

研究者

发起方
WHO

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