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 @ 11:38 PM
Ignite Modification Date:
2025-12-24 @ 11:38 PM
NCT ID:
NCT04199156
Eligibility Criteria:
Inclusion Criteria:
* full term singleton pregnant women (18-35 years) scheduled for elective cesarean delivery under spinal anesthesia.
Exclusion Criteria:
* Patients with coarctation of aorta,
* cardiac arrythmia,
* impaired cardiac contractility (ejection fraction\< 50%),
* congenital heart disease,
* moderate to severe valvular heart disease,
* uncontrolled hypertension,
* known peripheral vascular disease,
* peripartum bleeding,
* body mass index \> 35
* Condition which preclude placement of blood pressure cuff on either limb (lymphedema, high risk of developing lymphedema, local skin damage, known vascular stenotic lesion, deep venous thrombosis)
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
35 Years
Study:
NCT04199156
Study Brief:
Protocol Section:
NCT04199156