However, we are expected to learn how to present effectively by observation, trial, and error. Remember that the purpose of the case presentation is to convey your diagnostic reasoning to the listener. By the end of your presentation the examiner should have a clear view of the patient's ...
clinical researchethicsrandomized controlled trialsThe rapidly growing numbers of new drugs, devices, and interventions have led to a dramatic increase in the trials needed to evaluate these new therapies in all areas of medicine, but most notably in cardiology. This specialty alone demonstrated a ...
Deep vein thrombosis(DVT) is the subject of hundreds of medical studies worldwide. You might seek outclinical trialsbecause your currentDVT treatmentisn’t working well. If you have afamily historyof DVT, taking part in a trial could help you find ways to prevent the condition. Clinical trial...
How to ensure clinical trial sensitivity in psychotropic drug development: A case studyClin Ther. 2005 Feb;27(2):252-4. Letterdoi:10.1016/j.clinthera.2005.02.005Sebastián VidelaMariano SustAnna FresquetJesús VilloriaClinical Therapeutics
We gave our platform a name that reinforced its more fundamental purpose — to bring the workflows of key clinical trial stakeholders (together, the “study team”) onto a common platform and help them work together as one. Already, we have seen enrollment rates shift for the better. On...
LINEA System applies cutting-edge technology and data to accelerate clinical trials with our Study Start-up Management System (SSMS), AcceleTrial™.
In any case, physical quality assurance (QA) must be an essential aspect of the trial to ensure that SABR is delivered accurately and in a comparable fashion in radiotherapy centres participating in the trial. The present paper tries to explore the balance between the QA cost and benefit for ...
Insights into how to conduct a clinical trial in the UKNew researchers may find starting and conducting clinical studies in the UK complicated and time-consuming. In this article, we describe our collective experiences and provide some pointers on how to navigate through the various committees and...
Nevertheless, CFDA would never want to see this awful phenomenon again. So, to protect the consumers' health and prohibit all false drug/medical devices entering into the market, CFDA was carrying out a thorough investigation and reorganization for manufacturers using false clinical trial data fro...
Why, what and when to adapt in clinical trials Traditionally, clinical trials have been run in three steps [1]: The trial is designed. The trial is conducted as prescribed by the design. Once the data are ready, they are analysed according to a pre-specified analysis plan. ...