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73 While treatment with a set dose of 60 mg of obatoclax mesylate over 24 hours every 2 weeks was well-tolerated and several patients maintained stable disease, no PR or CR was observed.
74 Twenty-two patientsed patients were administered a set dose of 60 mg of obatoclax mesylate over 24 hours every 2 weeks, with the option of dose reduction to 45 mg if dose-limiting toxicities were observed.
Prandial insulin was also adjusted weekly based on pre-lunch, pre-dinner and bedtime self-monitoring of blood glucose results from the previous week, with the simple algorithm providing a set dose of insulin to inject preprandially, and the carbohydrate-counting algorithm providing a dose per amount of carbohydrate in the meal.
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A set of dose limitations were defined for the organs at risk depending on the standard of TD5/5, the dose at which, under standard treatment conditions, less than or equal to 5% of patients experienced serious complications within 5 years after radiation therapy, and the distance of the PTV to the organs at risk.
The optimal design is therefore a set of dose levels and weights.
Specifically, the percent volume receiving above a set high dose level (in this study, 60 Gy) was analyzed.
This device consists of a volumetric pump, which delivers a set intravenous dose of drug when a control button is pressed.
Patients completed a questionnaire that incorporated questions from standard psychometric instruments and a set of dose adjustment for normal eating (DAFNE) plates, which provide standardized photographs of meals with known CHO values (16).
Here we refer to priming effect as a set of dose-response behaviors: (1) A single low dose stimulant (LD) cannot activate the readout x3 (< 0.1 in a reduced unit with 1 the maximum induction).
Phase I clinical trials are conducted in order to find the maximum tolerated dose of a given drug out of a set of doses, usually finite.
Implementation requires a choice of a set of doses, a statistical model to describe the relationship between the probability of toxicity and the dose, a set of prior probabilities for toxicity at each dose, and a target 'acceptable' toxicity probability.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com