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 @ 2:14 PM
Ignite Modification Date:
2025-12-24 @ 2:14 PM
NCT ID:
NCT05308095
Description:
Any requests for raw data will be reviewed by the HEADWIND scientific study board comprising the principal investigator (PI) and Co-PI as well as senior researchers leading the involved research groups at University Hospital Bern, Swiss Federal Institute of Technology (ETH) Zurich, and University of St. Gallen. Only applications for non-commercial use will be considered and should be sent to the PI. Applications should outline the purpose for the raw-data transfer. Any data that can be shared will need approval from the HEADWIND scientific study board and a Material Transfer Agreement in place. All data shared will be de-identified.
Study:
NCT05308095
Study Brief:
The HEADWIND Study - Part 4