Which statement is true about trial-related injury is required in the consent?

• A. Details about compensation or treatment for trial-related injury.
• B. The schedule of visits only.
• C. The clinician's personal contact number.
• D. A statement that no injury will occur.

Answer: (B)

Informed consent must openly inform participants about what could happen to them, including any trial-related injuries and what would be done if such an injury occurs. The statement that details about compensation or treatment for a trial-related injury belong in the consent is the one that reflects this requirement. Participants need to know that if harm arises, there is a plan for medical treatment and, if applicable, compensation.

Information about the schedule of visits alone does not address risks, protections, or what happens if an injury occurs, so it doesn’t fulfill the requirement to inform about trial-related injuries. The clinician’s personal contact number is not a standard, required item in the consent form, and a statement that no injury will occur is inappropriate because it implies guarantees about risk that are not possible in research.