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The National Cancer Institute created the Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) to allow direct input on symptomatic adverse events (AEs) from adult patients in oncology trials.
Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events.
Validity and Reliability of the US National Cancer Institute's Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE).
The validity, usability, and scalability of the Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events prototype are currently being examined in academic and community-based settings.
In order to improve the accuracy and efficiency of collecting and grading adverse event data, the NCI has established the Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) measurement system [4, 5, 6, 7].
The US National Cancer Institute (NCI) has developed the Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) to capture patients' self-reported symptomatic adverse events in cancer clinical trials.
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As a companion to the CTCAE, NCI has developed a Patient-Reported Outcome version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) [8].
Patients received 60 Gy intensity modulated radiation therapy with concurrent weekly cisplatin (30 mg/m2), and reported the severity of their xerostomia/dysphagia (before and after treatment) using the patient-reported outcome version of the Common Terminology Criteria for Adverse Events (CTCAE) (PRO-CTCAE).
Children who heard the original, positive-outcome story were three times more likely to tell the truth than the children who heard the new, negative-outcome version.
In this positive outcome-driven version of Jocky's life we would observe him being humiliated by crafty cockney Bristow as the effects of vodka and dartitis took hold.
The Palliative care Outcome Scale – version 1 will be used with patients and family caregivers to measure quality of life and perceived symptoms of patients.
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