Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 1:24 AM
Ignite Modification Date:
2025-12-25 @ 1:24 AM
NCT ID:
NCT03475693
Eligibility Criteria:
Inclusion Criteria:
* • Age 12 to 18 years
* • Presenting chief complaint of headache, head injury, or concussion within the first 48 hours of injury.
* • GCS \> 13 on arrival.
Exclusion Criteria:
* • Age \< 12 years or \> 18 years
* • Inability to provide informed consent
* • Vomiting \> 2 episodes following injury
* • Physical or mental disability hindering adequate response to assessment of symptoms
* • Hemodynamic instability/medical condition requiring further acute life-saving medical intervention
* • Known brain mass, intracranial hemorrhage, skull fracture
* • Known contraindications to magnesium use
* • Known contraindication to Zofran use
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
12 Years
Maximum Age:
18 Years
Study:
NCT03475693
Study Brief:
Protocol Section:
NCT03475693