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Clinical Trial Summary

The primary aim of this research protocol is to compare if there is a difference in progression free survival between weekly versus 5-day 3 weekly cisplatin based chemotherapy regimen in women with locally advanced cervical cancer. The secondary aims are to compare quality of life assessment of patients and their carers as well as toxicity profiles both acute and late.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00548821
Study type Interventional
Source National University Hospital, Singapore
Contact Johann Tang
Phone 677204870
Email Johann_Tang@mail.nhg.com.sg
Status Not yet recruiting
Phase Phase 3

See also
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