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Efficacy was evaluated from patient micturition diaries.
Drug efficacy was evaluated in patients 2 h post-dose.
Efficacy was evaluated by liver biopsy and serologic markers.
The antitumor efficacy was evaluated using HepG2 cells-bearing nude mice.
Efficacy was evaluated by measuring the reduction of the mean tumor weight relative to mock control (P < 0.01).
Efficacy was evaluated using systematic review and meta-analysis (SR-MA) methodology.
Patients were allowed to take frovatriptan as symptomatic medication, whose efficacy was evaluated at the two hours pain-free rate.
The efficacy was evaluated as completely headache free, markedly effective (attack reduction >75%), effective (reduction >50%) or invalid (reduction <50%).
The SLED run efficacy was evaluated by the online KT/V data delivered by the dialysis system.
The protective efficacy was evaluated by the survival against lethal challenge with A. pleuropneumoniae serotype 1.
Learning efficacy was evaluated with a pre-post intervention measurement using a domain-specific questionnaire.
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