Infections, Papillomavirus Clinical Trial
Official title:
Gynaecological Follow-up of a Subset of 580299/008 Study Subjects
This study is designed to provide up to four years of annual oncogenic HPV DNA testing and
cervical cytology examination for NCT00122681 study subjects who displayed normal cervical
cytology but tested positive for oncogenic HPV infection at their last NCT00122681 study
visit (Visit 10, Month 48).
This follow-up study will also be offered to subjects who were pregnant at their last
NCT00122681 study visit (Visit 10, Month 48) so that no cervical sample could be collected at
that visit.
The objectives & outcome measures of the primary phase (study 008/580299) are presented in a
separate protocol posting (NCT00122681).
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Phase 1 |