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 @ 1:25 AM
Ignite Modification Date:
2025-12-25 @ 1:25 AM
NCT ID:
NCT06885593
Eligibility Criteria:
Inclusion Criteria:
* ASA 2
* Uncomplicated pregnancy
* Height between 150 cm-180 cm
* Signed the informed consent form
* 8 hours of fasting before the operation
* Patients who refuse normal delivery
Exclusion Criteria:
* Obstetric comorbidities affecting caval compression of the aorta
* Transverse development
* Fetal macrosomia
* Uterine anomaly
* Polyhydramnion
* Oligohydroamnion
* Membrane ruptures
* Intrauterine growth retardation
* Mothers with hyperactive lung disease
* Those with autonomic neuropathy
* Kidney failure
* Smokers
* Severe scoliosis or kyphosis
* Multiple pregnancy (twins, triplets,...)
* Those who do not reach T6 sensory block level after 10 minutes
* Those undergoing general anesthesia or IV analgesics for any reason
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT06885593
Study Brief:
Protocol Section:
NCT06885593