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 @ 12:44 AM
Ignite Modification Date:
2025-12-25 @ 12:44 AM
NCT ID:
NCT05098067
Eligibility Criteria:
Inclusion Criteria:
* Pregnant women in the first trimester (0-14 weeks gestation)
* Presenting to the emergency room at Women \& Infants Hospital in Rhode Island with a chief complaint of nausea and vomiting
* English or Spanish speaking
* Have not taken an anti-emetic such as Reglan or Zofran within the 6 hours prior to presentation
Exclusion Criteria:
* Allergy to Reglan, capsaicin or Zofran
* Another identifiable source for nausea and vomiting (i.e. gastritis, COVID, diabetic ketoacidosis)
* Molar pregnancies,
* Patients with a history of gastroparesis
* Patients with a history of preexisting diabetes mellitus
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT05098067
Study Brief:
Protocol Section:
NCT05098067