The Registry for Equal Access to Clinical Trials in Alzheimer’s study will work to overcome barriers to recruiting patients for Alzheimer’s and dementia clinical studies by using telehealth to ...

For instance, the NIH wrote on Oct. 19 to a Johns Hopkins University researcher to note that the institution is required to post the results of a clinical trial for which the agency provided grant ...

Most governments host health organizations responsible for tracking and overseeing clinical trials, and as a part of clinical trial registration, all funders must be reported in detail.

Clinical Trial Registration: The process of documenting a clinical trial's objectives, methodology, and outcomes in a publicly accessible database before the trial begins.

In the second part of a two-part series, “Research Roundtable” highlights additional elements of the “Study Registration” FAQ section from ClinicalTrials.gov. The Responsible Party is responsible for ...

Registration is required for studies that meet the definition of an "applicable clinical trial" (ACT) and either were initiated after September 27, 2007, or initiated on or before that date and ...

Trial registration: The process of recording the details of a clinical trial in a publicly accessible database, allowing for transparency and accountability in research conduct.

SUPPLEMENTARY INFORMATION: Back to Top HHS published a Notice of Proposed Rulemaking (NPRM) on Clinical Trials Registration and Results Submission in the Federal Register on November 21, 2014 (79 FR ...