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:
2025-12-24 @ 4:49 PM
Ignite Modification Date:
2025-12-24 @ 4:49 PM
NCT ID:
NCT07120750
Description:
1. Data Availability: De-identified individual participant data will be made available upon reasonable request after the completion of the study and publication of the primary results.
2. Time Frame: Data will be available starting from six months after the publication of the primary study results and for a period of five years thereafter.
3. Access Criteria:
(1) Requests for data access will be reviewed by the study's data monitoring committee.
(2) Data will be shared for research purposes that are consistent with the original study objectives and for the advancement of scientific knowledge.
(3) Researchers requesting access must submit a detailed proposal outlining their research question, methods, and analysis plan.
4\. Data Sharing Process:
1. Data will be provided in a de-identified format, ensuring participant confidentiality.
2. Along with the data, relevant documentation such as the study protocol, statistical analysis plan, and data dictionary will be made available to facili
Study:
NCT07120750
Study Brief:
Post-Radical Treatment Antiviral Strategies in HBV-Related Liver Cancer: Impact on Tumor Prognosis