Примери за използване на Study evaluated на Английски и техните преводи на Български
{-}
-
Medicine
-
Colloquial
-
Official
-
Ecclesiastic
-
Ecclesiastic
-
Computer
This study evaluated the efficacy of Me.
How are the results of an antro-duodenal motility study evaluated?
This study evaluated the efficacy of Me.
How are the results of an antro-duodenal motility study evaluated?
Only one study evaluated the efficacy of CPA/EE(2mg/0.035mg) versus placebo.
Antisocial personality disorder How are the results of an antro-duodenal motility study evaluated?
This study evaluated non-splenectomised patients with ITP and platelet counts< 50 x 10.
SURVEYOR-2 Part 3 was an open-label study randomizing non-cirrhotic treatment-experienced subjects to 12- or 16-weeks of treatment;in addition, the study evaluated the efficacy of Maviret in subjects with compensated cirrhosis and genotype 3 infection in two dedicated treatment arms using 12-week(treatment-naïve only) and 16-week(treatmentexperienced only) durations.
This study evaluated the chemistry and antioxidant properties of four commercial amla fruit extracts.
An open-label, non-comparative, multi-centre study evaluated 14 male patients(aged 2 to 9 years) with familial male-limited precocious puberty, also known as testotoxicosis, treated with combination of Arimidex and bicalutamide.
The study evaluated the mean symptom score using the change from baseline to the end of treatment.
An observational case-crossover study evaluated the risk of NAION when PDE-5 inhibitor use, as a class, occurred immediately before NAION onset(within 5 half-lives), compared to PDE-5 inhibitor use in a prior time period.
The study evaluated 284 mg inotersen administered as one subcutaneous injection once per week, for 65 weeks of treatment.
A study evaluated that daily intake of 100 milligrams of vitamin C plays in the urinary infection treatment during the pregnancy.
One study evaluated a topical preparation of turmeric, noting significant improvement in symptoms over the nine-week course of treatment.
Another study evaluated the influence of hatha yoga practice on levels of distress in women about to begin a course of in vitro fertilization(IVF).
This study evaluated the effectiveness of magnetic mattress pads in easing the muscle pain, stiffness and fatigue associated with fibromyalgia.
A study evaluated the effect of a single intravenous dose of 140 mg Aimovig in subjects with stable angina under controlled exercise conditions.
This study evaluated the safety, efficacy and convenience of TIP vs TIS in CF patients aged 6 years and above with chronic P. aeruginosa infection.
A study evaluated the pharmacokinetics of eribulin in patients with mild(Child-Pugh A; n=7) and moderate(Child-Pugh B; n=4) hepatic impairment due to liver metastases.
This study evaluated Kyprolis at an initial dose of 20 mg/m2, which was increased to 27 mg/m2 on cycle 1, day 8, administered twice weekly for 3 out of 4 weeks as a 10 minute infusion.
The study evaluated 11 years of data from the Food and Drug Administration(from 2003 to 2013) and found lead in 20 percent of baby food samples compared to 14 percent of other foods.
The study evaluated 234 adult patients with active rheumatoid arthritis who had failed therapy with at least one but no more than four disease-modifying antirheumatic drugs(DMARDs).
The study evaluated whether different genotypes- possible genetic combinations of the OXTR- influenced how spouses support one another, which is a key determinant of overall marital quality.
Case-crossover study evaluated the risk of NAION when PDE5 inhibitor use, as a class, occurred immediately before NAION onset(within 5 half-lives), compared to PDE5 inhibitor use in a prior time period.
The study evaluated the effect of adding Avastin to carboplatin+paclitaxel and continuing Avastin as a single agent until disease progression or unacceptable toxicity compared to carboplatin+paclitaxel alone.
This study evaluated Kyprolis at an initial dose of 20 mg/m2, which was increased to 56 mg/m2 on cycle 1, day 8, administered twice weekly for 3 out of 4 weeks as a 30 minute infusion until progression or unacceptable toxicity.
This study evaluated older adults every year for five years, and the executive function of those testing positive for toxoplasma seemed to drop quicker over time, as did a measure of their overall mental status.
While this study evaluated pembrolizumab as stand-alone therapy, other KEYNOTE studies have shown that combining the drug with chemotherapy or other treatments increases survival even more, based on early results, Eder said.
This study evaluated the efficacy of IV tocilizumab 4 or 8 mg/kg every 4 weeks/MTX combination therapy, IV tocilizumab 8 mg/kg monotherapy and MTX monotherapy in reducing the signs and symptoms and rate of progression of joint damage for 104 weeks.