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To assess blinding, at the end of the forty minute study period, the experimenter asked each subject open ended questions about what occurred during each study period.
If patients did not attain target range SBP within the 30 minute study period, rescue medications could be given at the physician's discretion.
If the participant does not complete the 60 minute study period, the reason for the premature termination will be documented on the CRF.
With the exception of the bottles of study drug, 2% viscous lidocaine may not be prescribed by the treating clinician during the 90 minute study period or for the preceding 90 minutes due to risk of lidocaine toxicity.
All adverse experiences either observed by the investigator or one of the clinical staff, or reported by the patient's parents/guardians spontaneously or in response to a direct question, that occur during the 60 minute study period, and the 30 minute observation period, will be evaluated by the investigator and noted in the adverse experience section of the patient's CRF.
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A small, nonsignificant increase in LIMA blood flow occurred during the 15-minute study period (30 ± 12 to 35 ± 10 mL/min) in patients who received fenoldopam.
Our study found that if a student checked Facebook just once during the 15-minute study period, he or she had a lower GPA.
At each time point during the 120-minute study period, vWF Ag/Hb was significantly higher in desmo-pressin-treated and AVP-treated animals than in vehicle-treated animals (P < 0.001 each).
Secondary outcomes were the difference in total minute ventilation (VE) in l/min (calculated as the sum of all breaths delivered during each one-minute study period), the occurrence f DMV (by Han's or Warters' scale), and a composite of MVi and/or Vds before and after the administration of NMBDs.
Without pharyngeal oxygen, the time to SpO2 below 60% was 103 (88 to 111) seconds, and with pharyngeal oxygen, three animals desaturated (after 55 seconds, 85 seconds, and 7 minutes), whereas the other five animals had adequate oxygenation during the whole 10-minute study period (P = 0.016).
Because previous data suggested a maximum decrease of tympanic temperature for CI (2.1 L within 35 minutes) after 52 minutes, a study period of one-hour was chosen.
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