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Patient-reported outcomes Carefully selected patient-reported outcome (PRO) instruments (standardised questionnaires designed to understand the patient experience) were administered at baseline and at 40 or 52 weeks across the SURPASS clinical trial programme (Boye et al, 2023)
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However, as observed in the SURPASS-5, daily insulin dose remained similar in participants randomized to TZP 5 and 10 mg and was mildly reduced in those assuming TZP 15 mg
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