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 @ 11:25 PM
Ignite Modification Date:
2025-12-24 @ 11:25 PM
NCT ID:
NCT03185156
Eligibility Criteria:
Inclusion Criteria:
* Patients aged 20-40 years;
* American Standards Association status I-II.
Exclusion Criteria:
* Patients with allergy or hypersensitivity to propofol, lipid emulsion, or granisetron;
* History of nausea or vomiting within 24h before cesarean delivery;
* History of gastrointestinal or psychiatric disease, motion sickness, smoking, postoperative nausea and vomiting;
* Morbid obesity;
* Consumption of drugs such as opioids, antiemetics , H2 antagonists, phenothiazines and/or corticosteroids within 24h before the study period;
* Any chronic medical or surgical disorders complicating the pregnancy;
* Conditions contraindicating regional anesthesia.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
40 Years
Study:
NCT03185156
Study Brief:
Protocol Section:
NCT03185156