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To evaluate the superiority of switching retrieval modes, it is compared with the random caching strategy (R-Caching) in terms of RTT and the number of interest packets.
Here we outline the PARADIGM study (NCT02394795), designed to evaluate the superiority of panitumumab over bevacizumab, in combination with oxaliplatin/5-fluorouracil/leucovorin (mFOLFOX6) in patients with RAS wild-type chemotherapy-naïve mCRC.
The feasibility of the proposed resilient virtual flux-based DPC (RVF-DPC) is verified by using MATLAB/Simulink and a comparative study is conducted to evaluate the superiority of the proposed controller with another three representative table-based DPC schemes.
The feasibility robustness index is utilized to evaluate the acceptability of a design vector as far as the constraint functions are concerned while the objective robustness index is utilized to evaluate the superiority and robustness of a design vector as far as the objective mechanical performance index is concerned.
Such a trial could also be designed to evaluate the superiority of active comparators.
However, a randomized controlled study is necessary to evaluate the superiority of DCGEM to gemcitabine monotherapy.
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We evaluated the superiority of the proposed method by checking whether the point of the proposed method was above the curve of the existing method or not.
We evaluated the superiority of directly observed therapy (DOT) for tuberculosis patients vs self-administered therapy (SAT) in decreasing ADR, microbiologic failure, and relapse in meta-analyses.
Another double-blind, randomized, Phase III trial evaluated the superiority of the combination of aprepitant and dexamethasone compared to metoclopramide plus dexamethasone in the prevention of delayed emesis in patients receiving cisplatin (single dose of ≥ 50 mg/m).
This study is designed as a non-blinded, multicentre randomised controlled, parallel-group trial evaluating the superiority of the BREATH intervention compared to usual care after primary curative breast cancer treatment.
EAGLE was a randomized, multicenter phase III study which evaluated the superiority of bevacizumab 10 mg/kg plus FOLFIRI compared with bevacizumab 5 mg/kg plus FOLFIRI in patients with mCRC previously treated with first-line bevacizumab plus an oxaliplatin-based regimen.
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