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| Methods | Randomized, double blind, placebo controlled | |
| Participants | n=41 FIGO stage IIB or IIIB ca cx | |
| Interventions | RT ‐ 40 ‐ 50Gy EBRT in 2Gy fractions followed by ICR & VR. Point A dose = 85Gy. HU ‐ 80mg/kg 3 x wk over 12 wks | |
| Outcomes | Acute chemotherapy toxicity NED rate | |
| Notes | Trial stopped as high proportion of 3b pts had PA node mets | |
| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Allocation concealment? | Low risk | A ‐ Adequate |
