In this paper we propose to use normalised design variables that inherently map (i.e. correspond) to feasible lamination parameters, effectively removing the need to evaluate feasibility constraints altogether.
This in turn means that for a trial with a fixed number of clusters, some designs will not be feasible, and we have provided simple guidelines to evaluate feasibility.
To evaluate feasibility and morbidity of a total laparoscopic radical hysterectomy (TLRH).
To evaluate feasibility and outcome of minilaparotomy hysterectomy in a consecutive series of patients.
To evaluate feasibility and results of automated perimetry in veterans with combat blast neurotrauma.
To evaluate feasibility and reliability of measuring saliva cortisol in athletes.
To evaluate feasibility, we designed a preliminary algorithm which we applied in a prograding delta environment.
Next they brainstormed solutions and built quick prototypes to evaluate feasibility, as well as risk factors such as intellectual property and the pathway to regulatory approval.
To evaluate feasibility, acceptability, continuation, and trough serum levels following self-administration of subcutaneous (sc) depot medroxyprogesterone acetate (DMPA).
To evaluate feasibility, advantages, and disadvantages of the laparo-endoscopic single site surgery (LESS) technique for balloon vaginoplasty (BV).
To evaluate feasibility and safety of MGuard based percutaneous coronary interventions (PCI) in vein grafts (VG) and native coronaries (NC).
