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 @ 3:37 AM
Ignite Modification Date:
2025-12-25 @ 3:37 AM
NCT ID:
NCT00237705
Eligibility Criteria:
Inclusion Criteria:
* Only patients who meet the following inclusion criteria will be recruited:
1. History of blunt head trauma within preceding 24 hours.
2. Immediate and transient post traumatic impairment of neurological functions defined as alteration of consciousness, amnesia, disorientation, disturbance of vision or equilibrium (10).
3. Onset of headache within one hour of trauma.
Exclusion Criteria:
* Patients with any of the following exclusion criteria will not be enrolled:
1. Age less than or equal to 19 years.
2. Known or suspected pregnancy.
3. Known hypersensitivity or intolerance to metoclopramide.
4. Inability to give informed consent.
5. Known gastrointestinal hemorrhage, perforation or obstruction.
6. Known seizure disorder.
7. Known pheochromocytoma.
8. Concurrent significant CNS depression due to drugs or alcohol.
9. Concurrent treatment for psychiatric illness.
10. Any acute brain injury on CT scan (if performed) as defined by any radiographic finding which would normally require admission to hospital and neurological follow up
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
19 Years
Study:
NCT00237705
Study Brief:
Protocol Section:
NCT00237705