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I think anything clinical should be passed to the doctor full stop.
Furthermore, outcome measures (both laboratory and clinical) should be standardized between studies to facilitate comparison.
Ideally, imaging studies (both preclinical and clinical) should be co-registered with linked genomic and proteomic information in order to fully interpret the biological relevance of the images obtained [ 404- 406].
Thus, the results from several different types of studies (experimental, epidemiologic, and clinical) should be moving in the same direction with consistency, to be useful for determining DRIs for individual nutrients.
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Existing clinical groups and clinical leadership should be utilized to influence antimicrobial prescribing behaviors.
Whether this translates to clinical efficacy should be assessed in further clinical studies.
As such, the clinical information should be used to guide individual clinical decisions.
Clinical practice should be guided by evidence from well designed clinical trials [ 1- 3].
While the clinical trials with TT are scarce, and randomized placebo controlled clinical trials should be done in future.
Numerous clinical questions remain, and enrolment of patients into well-designed clinical trials should be encouraged.
Clinical trials should be performed to ascertain the effectiveness of this technique in clinical practice settings.
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