1.(Medicine)medan inactive substance or other sham form of therapy administered to a patient usually to compare its effects with those of a real drug or treatment, but sometimes for the psychological benefit to the patient through his believing he is receiving treatment. See alsocontrol group,pl...
RegisterLog in Sign up with one click: Facebook Twitter Google Share on Facebook Dictionary Medical Acronyms Encyclopedia Wikipedia </>embed</> Roman Catholic Western Church Roman Church Roman Catholi... Church of Rome vesper (Roman Cathol... ...
making paper sailboats with my brother…. Placing my fingers in a bowl of water and stroking a paper sailboat enabled me to participate in the total experience… I felt tingling sensations all over my body, like tiny bundles of energy exploding inside of me. By the end of the week the si...
The primary outcome was effect at week 12 on the PANSS Total Score. Effects on the MATRICS, other PANSS subscales, Clinical Global Impression, and Global Assessment of Functioning were secondary outcomes. There were no observed treatment effects on any behavioral outcome measure. Baseline C-...
The primary outcome was hemodynamically significant PDA closure within 1 week of administration of the first dose of the intervention and defined echocardiographically (as physical closure of PDA or change from hemodynamically significant to nonsignificant status based on a priori–defined parameters) or ...
Volunteers were included who had not used any psychotropic medications or hormone treatments for at least 1 year, had no history of smoking, and did not exercise in excess of 1 hour 3 times a week. Women had regular menstrual cycles of 26 to 32 days' duration and had not used hormonal ...
Here, the potential for this error was reduced by combining intervention groups and focussing on 16-week analyses only. However, no analyses in this trial produced a statistically significant result. The direction and magnitude of effects were exam- ined for meaningful trends, but none were found...
The feasibly of the 1% sirolimus treatment in SOTRs by reviewing completion of the 24-week application course, total number of doses applied during the course, cost of treatment (whether topical sirolimus therapy or current standard of care + placebo), quality-adjusted life years (QALY’s...
This 8-week, randomized, placebo-controlled, dose-escalated trial was conducted to determine the effect of GG on blood safety and hormone markers in healthy adults. Sixty-six males and females between 30 and 49 years of age were supplemented with either GG or a placebo (PLA) for 8 weeks,...
week period. Our study served as a pilot and was strengthened by the serial exposure to a placebo and then a probiotic. Therefore, each person served as their own control, and this increased the overall power of the study. Future studies with acne should build upon the pilot results here ...