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 @ 3:20 PM
Ignite Modification Date:
2026-03-26 @ 3:20 PM
NCT ID:
NCT07458620
Description:
1. Data Protection and Retention Limits: The protocol strictly mandates that all de-identified data and specimens will be destroyed five years after the formal conclusion of the trial.
2. Privacy and Confidentiality: To protect the privacy of participants, data is stored under locked and encrypted conditions, with access restricted to the immediate research team members.
3. Restricted Future Use: While participants can consent to have their data stored in the hospital's internal biobank, this authorization is limited specifically to future research within Kaohsiung Chang Gung Memorial Hospital and does not extend to public or external sharing.
4. Legal Representative Consent: Because the study involves participants with cognitive impairments who may lack the capacity to exercise autonomy, data management is subject to strict ethical oversight that prioritizes the protection of the participants' rights over broad data dissemination.
Study:
NCT07458620
Study Brief:
Prospective Single-Arm Safety Study of Cervical LVA in AD Patients