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{x i } and (hat {n}) stand for either (left {x^{(c)}_{i}right }) and n c or (left {x^{(t)}_{i}right }) and n t, and (left {x^{(c)}_{i}right }) (i=1…n c ) and ({x^{(t)}_{i}}) (i=1…n t ) are logarithmically transformed measured trial variables.
By using epidemiological and cost data external to the trial, we were able to extrapolate from directly measured trial outcomes (DV disclosure and referral rates) to QoL, health and economic outcomes.
By using epidemiological and cost data external to the trial, we were able to extrapolate from directly measured trial outcomes (DV disclosure and referral rates) to quality of life, health and economic outcomes.
For costs associated with events beyond the measured trial outcomes (identification and referral to DV advocacy), estimations were drawn from Walby's analysis of the societal and personal costs incurred by women experiencing abuse (table 3).
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While it could be argued that this might influence the findings presented in this paper (e.g. number of publications/population favours the production of smaller trials), we hope to have avoided measuring trial participation.
This will include measuring trial recruitment rate, including recruitment to each factorial comparison separately.
Serum creatinine and cystatin C were measured at trial end and 6 8 weeks after discontinuation of trial therapy.
The required amount of tamping for target density was measured by trial method.
(A) Spleen to body mass ratios were measured upon trial conclusion (8 weeks).
Unreported secondary outcomes were either not measured (two trials), measured but not analysed (12 trials), or measured and analysed but not reported (eight trials).
Design: This study was a clinical, prospective, open, repeated measures trial, with data collection between January and July 2015.
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