... to identify important harms. Use consistent and precise terminology ... when clinical trials are lacking; when generalizability is uncertain; or when ...

... information exchanges of different purposes, including registries and clinical trials, quality initiatives, safety, and public health reporting. 23 Content profiles such as Clinical Research Data ...

... allows registries to become specialty and sub-specialty reporting mechanisms under the Qualified Clinical Data Registry (QCDR) Program. 43 In this capacity, professional societies, particularly sub- ...

... an RCT is unlikely to be relevant to clinical treatment, where it is important to recognize the individual’s needs. Some trials evaluated manualized programs for which resources and training are available (e. ...

... D.M., Robichaud, J.A., Two-year exercise program improves physical function in Parkinson’s disease: The PRET-PD randomized clinical trial, Neurorehabilitation and neural repair, 29, 112–122, 2015 ...

... care in primary care, specifically the Positive Parenting Program (Triple P), which has been shown to be effective in clinical trials. The study assigned four community-based, hospital-affiliated ...

... categories (see Figure 9 ). For the purposes of clinical reporting, additional comments can describe SDV findings in more detail. The new classification incorporates appropriate existing terminology, such as the classification of spinal abnormalities of ...

... HPV DNA on cervical cytologic specimens and their clinical validity for identification of precancerous lesions or cervical cancer. Terminology for Cervical Lesions In the United States, most laboratories use the Bethesda system for reporting cervical cytology ( Table 1 ). The classification system was ...

... medical interventions: AHRQ and the effective health-care program. J Clin Epidemiol. 2010 May; 63 (5):502–12. [ PubMed : 18823754 ] 57. Ioannidis JP, Lau J. Improving safety reporting from randomised trials. Drug Saf. 2002; 25 (2):77–84. [ PubMed : ...

... used approach to classifying lymphedema is the Common Terminology Criteria for Adverse Events v3.0 (CTCAE), which were developed for grading adverse events in the context of clinical trials.[ 37 ] A key advantage of the CTCAE approach ...