Clinical Trials are research studies on new drugs, surgical procedures, and medical devices. According to the National Institutes of Health (NIH), over 300,000 clinical trials are registered worldwide, with over 40,000 in the United States alone. These trials cover various medical interventions, including drugs, surgical procedures, and medical devices. These trials effectively ensure that any new…
During data collection and data entry in a medical research study, errors can occur. Research coordinators handling the shifting of the data might make a mistake in transforming them from paper-based formats to digitized ones. If these errors are left standing and not identified before analysis, they can distort the outcome of the clinical trial, which will…
Electronic Patient-Reported Outcomes, or ePROs, are a type of electronic data-capturing method mainly used in clinical research and the healthcare system. Patient-reported outcomes (PROs) are any aspect of a patient’s health status that is reported by the patient directly, excluding any interpretation done by a professional along with the way. ePROs is the technology that uses…
While there are certain set criteria that exclude patients from participating in clinical trials, and many times researchers themselves have parameters, it’s also important to look at the flip side. For a clinical trial to be truly successful, it needs a comprehensive EDC software program and a concerted effort to carry out inclusive and ethical research. Here are…
Clinical trials are a significant component that improves patient care and advances medical research. Data management in clinical trials provides valuable insight into new interventions and treatments. An increasingly popular aspect of these trials is patient data registries. A patient data registry is a centralized form of database related to patients with a specific disease or…
With time, research organizations are becoming more efficient and patient-centric. The current research methodology embraces technological advancements and explores remote options. The COVID-19 pandemic has been critical in taking the research industry towards a virtual, flexible approach from the traditional brick-and-mortar site. This is where the decentralized clinical trial (DCT) model comes in, and today…
Did you know that over $2.6 billion is spent on clinical trials? Many pharmaceutical corporations and research institutions use clinical trial management systems (CTMS) to control these expenses and guarantee the timely completion of clinical trials. At a CAGR of 11.4%, the market for clinical trial management systems is anticipated to increase between 2022 and 2030.…
You may acquire and store data digitally using the effective data-collecting technique known as Electronic Data Capture (EDC). Data may be gathered from various sources, including paper forms, digital forms, and mobile devices, with the help of EDC, which is simple to use. To enter data, organize a database, and conduct analysis for clinical trials, clinical…
Before beginning your study, you must select a suitable clinical trial management system (CTMS) Vendor that can not only benefits your research organization but is also patient-centric. When you’re in the market for an appropriate CTMS, you should look for one that fits well with your research goals and meets all your requirements. To that…
A screen failure in clinical trials happen when potential participants undergo a screening process designed to determine whether they fit the study’s inclusion criteria, and despite fitting the criteria, they fail to enroll in the trial. While there’s no standardized screen failure information for different studies, some studies show a higher incidence of screen failure.…