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 @ 11:50 PM
Ignite Modification Date:
2025-12-24 @ 11:50 PM
NCT ID:
NCT05998551
Eligibility Criteria:
* Inclusion criteria:
* Multiparous women who received antenatal care, presented for vaginal delivery of uncomplicated term pregnancy of singleton fetus with engaged fetal head and cervical dilatation of at least 5 cm requiring oxytocin augmentation, and requested analgesia.
* Age: patients between 22-45 years old.
* Exclusion criteria:
* Refusal of procedure or participation in the study.
* Patients with pre-existing or pregnancy-induced hypertension, abnormal fetal heart rate tracings, obesity, endocrinal diseases and/or diagnosed fetal abnormalities.
* Contraindication to neuraxial block.
* Allergy to any of the study drugs.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
22 Years
Maximum Age:
45 Years
Study:
NCT05998551
Study Brief:
Protocol Section:
NCT05998551