Protocol Section
The Protocol Section is one of the main sections in ClinicalTrials.gov data structure. It contains protocol-related information for clinical trials, including identification, status, design, eligibility, and other key details about how the trial is structured and conducted.
Protocol Section path is as follows:
Study -> Protocol Section -> Protocol Modules (Identification, Status, Design, Eligibility, etc.)
Protocol Section
Ignite Creation Date:
2026-03-26 @ 3:21 PM
Ignite Modification Date:
2026-03-26 @ 3:21 PM
NCT ID:
NCT05412927
Description:
The study doctor will collect your personal and medical information. For example:
* Past and present medical records
* Research records
* Records about phone calls made as part of this research
* Records about your study visits
Your information may be given to:
* The U.S. Food and Drug Administration (FDA),
* Department of Health and Human Services (DHHS) agencies,
* Governmental agencies in other countries,
* Governmental agencies to whom certain diseases (reportable diseases) must be reported
* Central IRB
Why will this information be used and/or given to others?
* to do the research,
* to study the results, and
* to see if the research was done right.
Study:
NCT05412927
Study Brief:
AngelMed Guardian® System PMA Post Approval Study