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1                                  New randomized, controlled trials have become available on oral P2Y(12) inhibitors in ac
2                                   Similarly, fewer clinical trials have been completed in PDAC (n = 608) compared with br
3                                 As of now, several clinical trials have been conducted to assess the benefits of TRT-base
4            To address this, several treatment de-escalation trials have been conducted, but only a few of these have prov
5                                           Numerous clinical trials have been launched to identify effective treatments fo
6                           Two blinded randomized controlled trials have been published, one with level I evidence (Yale-B
7 gnant adults, few published data from randomised controlled trials have compared the safety and efficacy of any integrase
8              Mendelian randomization studies and randomized trials have conclusively demonstrated that lower low-density
9                                                    Clinical trials have demonstrated health status benefit of transcathet
10                                         Randomized clinical trials have demonstrated that catheter ablation for atrial fi
11                                              Well-conducted trials have demonstrated that long-term opioid agonist therap
12 s haematopoietic stem cell transplantation, and prospective trials have demonstrated the potency of immunotherapeutic app
13                                Numerous randomized clinical trials have demonstrated the superiority of thin-strut biodeg
14                                      Meta-analyses of these trials have established the safety of statins with regard to
15                                        More recent clinical trials have focused on conditions mediated by LLPCs and have
16                                                        Some trials have found that patients from the United States derive
17                                        Community randomised trials have had mixed success in implementing combination pre
18 get specific immune pathways, and findings from prospective trials have indicated that less-restrictive, empiric, elimina
19                             Nonetheless, data from clinical trials have led to the approval of the XPO1 inhibitor selinex
20 peutic options for metastatic UM are limited, with clinical trials having little impact.
21 ate latent HIV in preclinical animal models and in clinical trials have measured HIV induction in the peripheral blood wi
22 ship of heart failure (HF) guideline citations and clinical trials have not been examined.
23 iologic plausibility and causality as randomized controlled trials have not been performed.
24                                              Multiple small trials have proposed that the administration of glucocorticoi
25 d therapy for hypertension, and randomized, sham-controlled trials have provided proof-of-principle data for its blood pr
26                                        Moreover, almost all trials have quantified treatment effects by using the hazard
27                                          Phase III adjuvant trials have reported significant benefits in both relapse-fre
28                                                     Earlier trials have revealed mixed outcomes and early outcomes from a
29                                          Two large clinical trials have shown a reduced rate of breast cancer development
30                                         Previous randomised trials have shown an overwhelming benefit of mechanical throm
31 are adjuvant therapy, although data from several randomized trials have shown improved outcomes with neoadjuvant treatmen
32                                           Although clinical trials have shown improvements in motor function in infants a
33 s with scalability and interdonor variability, and clinical trials have shown inconsistent outcomes(3,4).
34              Outcome data from procalcitonin-guided therapy trials have shown similar mortality, but the essential questi
35                                                  Randomized trials have shown that initiating breast cancer screening bet
36 n or other indications for anticoagulation, recent clinical trials have shown the benefit of double therapy with full-dos
37  targets within the immune pathogenic process, and the four trials have similarities and differences that mean they might
38                                    Results from more recent trials have stimulated a renewed interest in hypofractionatio
39                                                 However, no trials have studied whether or when women can safely stop scr
40 in preclinical models of neonatal brain injury, and phase 2 trials have suggested possible efficacy; however, the benefit
41 lerated fibrosis progression, yet few randomized controlled trials have tested clinic-based alcohol interventions.
42                             Though several hundred clinical trials have tested immune-based approaches in childhood cance
43                                  Four randomised controlled trials have tested the efficacy of three new therapies (eculi
44                                           North American HF trials had the highest likelihood of having a woman as first
45 ues: (1) how to effectively and efficiently determine which trials have the best chance of benefiting current and future
46 gs that have already advanced through human clinical safety trials have the potential to be approved more quickly than de
47                                              Early clinical trials have thus far focused on safety and target engagement
48                                                       These trials have used the noninferiority trial approach.
49                         Findings from randomized controlled trials have yielded conflicting results on the association be
50                                      Although some clinical trials have yielded promising results, others have shown no c