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Conclusions: This trial confirmed the efficacy of citalopram 40 mg per day, and clearly supports the use of citalopram infusion in the treatment of severely depressed, hospitalised patients.
This trial confirmed another three important aspects.
This trial confirmed the excellent safety results reported in C-98-03 C-98-03 C-98-03
This trial confirmed the safety of the combination drug and the best improvement was seen at the highest dose.
Again, this trial confirmed the notion that initially intensive regimens do not induce a superior outcome compared to well tolerated single-agent first-line strategies.
The toxicity data from this trial confirmed the previous results of low uterine toxicity for raloxifene, with a significant reduction in the incidence of endometrial hyperplasia, atypia and the requirement for hysterectomy.
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The revelations from this trial confirm that the system is indeed fixed.
The results of this trial confirm the antiviral activity of BCV against adenoviruses.
This trial confirms that the GET regimen can be safely administered at full doses with a few patients requiring dose adjustments.
The results from the 24-week, placebo-controlled, double-blind phase of this trial confirm the previously reported efficacy of one course of intravenous ofatumumab in active RA.
The results from this trial confirm that a short course of dose-dense weekly NACT with carboplatin and paclitaxel, followed by radical CRT, is feasible with acceptable toxicity.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com