The SWOG S2302 Pragmatica-Lung trial, which broke new ground with its streamlined pragmatic design, unusually broad eligibility criteria, and reduced data collection, has quickly answered its primary ...

We determined inclusive, contemporary estimates of clinical trial participation for adults with cancer using a national sample of data from the Commission ... according to the research plan or ...

Background Pulmonary hypertension (PH) is a progressive cardiopulmonary condition associated with increased morbidity and ...

Five deals that showcase the potential dealmakers see in the surgical equipment segment. Ampersand Capital, PAI Partners and ...

Importantly, almost half the steps involved in protocol activation in the study of the academic center ... train the research nurses and data coordinators and the clinical research unit personnel, and ...

In calling for more clinical testing of vaccines in younger people and those who face a low risk of severe disease from Covid ...

The International Severe Acute Respiratory and emerging Infections Consortium (ISARIC)–WHO Clinical Characterisation Protocol UK (CCP-UK) study is an ongoing prospective multicentre cohort study being ...

Time to trial activation (TTA) is the time from receipt of a clinical trial protocol and the activation of the clinical trial site to enrol research subjects and includes the entirety of approval ...

The study protocol is registered with the China Clinical Trial Registry (ChiCTR2400086452 ... Using these values in the formula, the required sample size per group (n) is calculated as 615, thus ...

eCOAs address these risks by digitizing the data collection process. Real-time data capture, logic checks and automated ...