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 @ 2:52 PM
Ignite Modification Date:
2025-12-24 @ 2:52 PM
NCT ID:
NCT06855459
Description:
Plan for Sharing Individual Participant Data (IPD)
* Data Sharing Statement: IPD will be shared as de-identified data, including study protocol, statistical analysis plan, informed consent form, and clinical study report.
* Timeframe: Data will be available within 6-12 months after publication and accessible for at least 5 years.
* Data Access: Stored in ClinicalTrials.gov, Vivli, or Dryad, data will be shared upon formal request with a research proposal. Requests will be reviewed by a Data Access Committee (DAC) based on scientific validity and ethical compliance.
* Privacy Protection: Data will be anonymized per HIPAA/GDPR standards, ensuring participant confidentiality.
* Usage: Available for meta-analyses and secondary research, with proper citation required. Commercial use is prohibited.
Study:
NCT06855459
Study Brief:
The Impact of Biophoton Therapy on Self-Grown Stem Cells