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 @ 11:52 PM
Ignite Modification Date:
2025-12-24 @ 11:52 PM
NCT ID:
NCT00846651
Eligibility Criteria:
Inclusion Criteria:
* American Society of Anesthesiologists (ASA) physical status I and II
* Elective cesarean section
* Weight 50-120 kg, Height 150-180 cm
* Normal singleton pregnancy
* Beyond 36 weeks gestation
* No known fetal abnormalities
* Ages 18-35
Exclusion Criteria:
* Contraindications to spinal anesthesia
* Multiple gestation, placenta previa, accreta
* Pregnancy induced hypertension or preeclampsia
* Diabetes mellitus, cardiovascular diseases
* Coagulopathy
* Spinal cord abnormalities, spinal surgery, or preexisting neurological dysfunction
* Baseline HR \<65
* Failed spinal anesthesia/inadequate sensory block for surgery
* History of abnormal bleeding
* History of adverse reactions to hydroxyethylstarch
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
35 Years
Study:
NCT00846651
Study Brief:
Protocol Section:
NCT00846651