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 @ 6:36 PM
Ignite Modification Date:
2025-12-24 @ 6:36 PM
NCT ID:
NCT06715657
Eligibility Criteria:
Inclusion Criteria:
* Parturient of American Society of Anaesthesiologists (ASA) class I or II physical status.
* Age: 20-40 years.
* At term gestation (≥ 37 weeks) with a singleton uncomplicated pregnancy.
* Elective cesarean delivery under intrathecal anaesthesia
Exclusion Criteria:
* Parturient refusal.
* Significant organ dysfunctions (e.g., cardiac, respiratory, renal, or liver disorders).
* Morbid obesity (BMI \>35).
* Parturient with known hypersensitivity to propofol, morphine or amide local anaesthetics.
* Parturient with pruritogenic systemic disease.
* A coexisting skin disorder or preexisting pregnancy induced pruritus.
* Parturient with any contraindication for intrathecal anaesthesia, e.g. coagulopathy.
* Emergency cesarean section.
* Failed or unsatisfactory intrathecal block.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
40 Years
Study:
NCT06715657
Study Brief:
Protocol Section:
NCT06715657