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:
2025-12-24 @ 2:30 PM
Ignite Modification Date:
2025-12-24 @ 2:30 PM
NCT ID:
NCT01785459
Eligibility Criteria:
Inclusion Criteria:
1. Age 18-65 years old
2. Diagnosis of benign or primary headache
Exclusion Criteria:
1. Hypersensitivity or allergy to bupivacaine (amide anesthetics) or prochlorperazine or other drugs in the same class, dopaminergic blockers.
2. Overlying signs of infection at site of injection (Erythema, purulence, open skin)
3. Neck pathology ( History of surgery to the cervical spine, History of surgical hardware in place, Documented disc abnormality, History of vertebral artery or carotid artery dissection, Torticollis)
4. Intracranial abnormality/pathology (Tumor, Hemorrhage, Concussion or post concussive syndrome)
5. History of increased intracranial pressure (ICP)
6. A known history of extrapyramidal symptoms, dystonia, parkinsonism, tardive dyskinesia or neuroleptic malignant syndrome
7. Known pregnancy
8. Narcotic seeking patients as determined by the treating physician with optional assistance from medical record review and North Carolina Drug Database
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT01785459
Study Brief:
Protocol Section:
NCT01785459