Voorbeelden van het gebruik van Placebo-controlled study in het Engels en hun vertalingen in het Nederlands
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In a 12-week placebo-controlled study with 54 patients with irritable bowel syndrome administration of twice daily 200mg palmithoylethanolamide
In this 5-week placebo-controlled study 63 patients received Sativex
The efficacy of Enbrel was assessed in a randomised, double-blind, placebo-controlled study in 205 patients with psoriatic arthritis.
A randomized and placebo-controlled study tracks 360 people that experience weight problems for 20 week.
The placebo-controlled study with Sativex has recruited 339 patients in the UK,
double-blind, placebo-controlled study evaluating efficacy endpoints at Week 6
The effectiveness of the composition has been proven by conducting a double-blind, placebo-controlled study.
double-blind, placebo-controlled study.
A randomized and placebo-controlled study tracks 360 individuals who experience from excessive weight for 20 week.
Results at Week 24(LOCFa) of a placebo-controlled study of dapagliflozin as monotherapy.
randomised, placebo-controlled study RHODOS.
In the placebo-controlled study, the rate of hot flushes was 1.0% for ulipristal acetate and 0% for placebo.
This was a double-blind, placebo-controlled study with only a short period of exposure(just 20 minutes) to saffron.
from baseline with alogliptin 25 mg at Week 26 by placebo-controlled study FAS, LOCF.
The efficacy and safety of lixisenatide in people aged≥70 years with type 2 diabetes was evaluated in a double-blind, placebo-controlled study of 24 weeks duration.
A randomized and also placebo-controlled study tracks 360 people that deal with weight problems for 20 week.
safety of empagliflozin as add-on to antidiabetic therapy was evaluated in patients with renal impairment in a double-blind, placebo-controlled study for 52 weeks.
12-week double-blind, placebo-controlled study.
A 26-week placebo-controlled study was designed to evaluate the efficacy
double-blind, placebo-controlled study compared zoledronic acid 4 mg to placebo for the prevention of skeletal related events(SREs) in prostate cancer patients.