Examples of using Randomised controlled in English and their translations into Croatian
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We included nine randomised controlled trials.
A randomised controlled trial to compare methods of milk expression after preterm delivery(Jones et al ADC 2001;85:F91).
In total, we analysed four randomised controlled studies with 4187 participants.
The use of Biatain Ibu for leg ulcers is supported by several randomised controlled studies(1-3).
Twenty-five randomised controlled trails were included in this review.
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This updated review includes 94(62 new to this update) randomised controlled trials involving 9821 participants.
We included 22 randomised controlled trials with 2503 participants, both men and women, between the ages of 18 and 65 years.
This adverse reaction was identified through post-marketing surveillance butnot observed in randomised controlled clinical trials n=6300.
There is a need for randomised controlled clinical trials to find out which treatment is most effective.
The safety profile of Omidria is based on data from 459 adult patients collected during clinical development obtained in randomised controlled trials.
At the moment there is only one randomised controlled study, which involved 256 women.
Randomised controlled data found no increased risk of coronary artery disease in hysterectomised women using oestrogen-only therapy.
Cetuximab as a single agent orin combination with chemotherapy was investigated in 5 randomised controlled clinical studies and several supportive studies.
We searched for randomised controlled trials that examined the effect of hypnosis for induction of labour.
As with many interventions intended to prevent ill health, the effectiveness of parachutes has not been subjected to rigorous evaluation by using randomised controlled trials.
More large-scale randomised controlled trials are needed before firm conclusions can be reached about the effectiveness of aromatherapy for dementia.
The frequency category was estimated from a statistical calculation based on the total number of patients exposed to nevirapine in randomised controlled clinical studies n=2,718.
The safety of Fampyra has been evaluated in randomised controlled clinical studies, in open label long term studies and in the post marketing setting.
The frequency category was estimated from a statistical calculation based on the total number of patients exposed to nevirapine in randomised controlled clinical studies n= 2,718.
In the pivotal randomised controlled study(D9902B, IMPACT, see section 5.1) Provenge was discontinued in 1.5% of patients due to adverse reactions.
The KRAS exon 2 status was recognised as predictive factor for the treatment with cetuximab in 4 of the randomised controlled studies EMR 62 202-013, EMR 62 202-047, CA225006, and CA225025.
We included six randomised controlled trials(RCTs), that is, studies in which participants are randomly allocated to one of two or more treatment groups.
This adverse reaction was identified through post-marketing surveillance for Eviplera(fixed-dose combination) butnot observed in randomised controlled clinical studies for Eviplera.
There is no evidence from randomised controlled trials of protection against myocardial infarction in women with or without existing CAD who received oestrogen-only therapy.
In June 2014 we searched for as many relevant medical studies as we could find that had a robust design(randomised controlled trials) that had compared hydrogel dressings with other treatments for pressure ulcers.
Antiviral efficacy data from randomised controlled studies is available for cobicistat-boosted atazanavir, but not for cobicistat-boosted darunavir see sections 4.4 and 5.2.
In addition, cetuximab was investigated in combination with chemotherapy in an investigator-initiated randomised controlled phase-III study COIN, COntinuous chemotherapy plus cetuximab or INtermittent chemotherapy.
Two randomised controlled studies were conducted in 270 haemodialysis patients and 288 patients not yet undergoing dialysis, who were on stable treatment with epoetin beta.
The safety of Bexsero was evaluated in 14 studies including 10 randomised controlled clinical trials with 8776 subjects(from 2 months of age) who received at least one dose of Bexsero.
The COPD clinical development programme included a 12-week(HZC113107), two 6-month(HZC112206, HZC112207) and two one-year(HZC102970,HZC102871) randomised controlled studies in patients with a clinical diagnosis of COPD.