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 @ 5:05 AM
Ignite Modification Date:
2025-12-25 @ 5:05 AM
NCT ID:
NCT07253818
Eligibility Criteria:
Inclusion Criteria:
* Term pregnant patients
* Singleton pregnancy at ≥37+0 weeks of gestation.
* Maternal age between 18 and 45 years.
* Hemodynamically stable and in sinus rhythm.
* Ability to provide verbal and written informed consent.
Exclusion Criteria:
* Hypertensive disorders of pregnancy, significant valvular or congenital heart disease, cardiomyopathy, or persistent arrhythmias.
* Multiple gestation (i.e., Twin pregnancy and above)
* Endocrine or hematologic conditions likely to affect hemodynamics, including diabetes with or without autonomic neuropathy, thyroid storm, or severe anemia (hemoglobin \<8 g/dL).
* Active labor with pain or current infusion of uterotonic or vasoactive agents.
* Ruptured membranes with frequent contractions or indications for emergent delivery.
* Inadequate transthoracic echocardiographic imaging windows at screening.
* Emergency or STAT (statim) Cesarean Deliveries
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT07253818
Study Brief:
Protocol Section:
NCT07253818