Exact(3)
All study designs (qualitative, quantitative randomized experimental, quantitative non-randomized controlled, quantitative observation, and mixed methods) were eligible for inclusion.
All six practices agreed to take part in stage 2, however only the four that employed systematic invitation methods were eligible.
Women between 30 and 70 years of age, with histologically confirmed endometrial hyperplasia according to WHO94 classification and D-score (see Additional methods) were eligible; excluded were women with hypersensitivity to progestin, active genital infection, a history of genital or mammary cancer, undiagnosed vaginal bleeding, liver disease, serious thrombophlebitis, or pregnancy.
Similar(57)
Women of reproductive age, registered at one of the local primary health care centres as users of a modern contraceptive method were eligible for this study.
Still, Mr. Verrilli said, the Prometheus method was eligible to be patented as an initial matter but could then probably be challenged as invalid because it was obvious and insufficiently novel.
It had urged the court to rule that the Prometheus method was eligible to be patented as an initial matter but could then probably be challenged as invalid because it was obvious and insufficiently novel.
Review methods Reviews were eligible if SMD results were based on two to ten randomised trials and if protocols described the outcome.
We did not limit our review to any particular type of study design – quantitative, qualitative and mixed method research were eligible for inclusion.
On the basis of sampling methods, 21,668 patients were eligible for enrollment in the etiology study and 10,746 enrolled (50% of eligible, 27% of all ALRI).
Trials involving the insertion of parenteral access under simulated conditions, such as using manikins or cadavers in which healthcare workers are randomly allocated to insert different parenteral access methods, were also eligible.
Methods and Results Patients were eligible if they had stable exertional angina, a significant reversible perfusion defect by stress myocardial perfusion study, and coronary anatomy that was suboptimal for percutaneous coronary intervention or coronary artery bypass grafting.
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