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 @ 11:11 PM
Ignite Modification Date:
2025-12-24 @ 11:11 PM
NCT ID:
NCT02760069
Eligibility Criteria:
Inclusion Criteria:
* ages 18 and older
* complaint of nausea and/or vomiting reported at 3 or above on verbal numerical rating scale at the time of triage
Exclusion Criteria:
* allergy to isopropyl alcohol or ondansetron
* inability to breathe through nose (e.g., recent upper respiratory infection)
* intake of cefoperazone, disulfiram, or metronidazole within the last 24 hours
* mental status precluding informed consent including intoxication
* known QT-prolongation
* clinical suspicion for serotonin syndrome
* intravenous catheter in place prior to study start
* medications administered since patient arrival (e.g., in triage)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02760069
Study Brief:
Protocol Section:
NCT02760069