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 @ 10:17 PM
Ignite Modification Date:
2025-12-24 @ 10:17 PM
NCT ID:
NCT05582135
Eligibility Criteria:
Inclusion Criteria:
* nulliparous parturients who scheduled for elective caesarean delivery under spinal-epidural anaesthesia;
* parturients who had requested postoperative analgesia;
* parturients aged between 20-35 years old;
* parturients who had a full-term pregnancy;
* parturients who were identified as having a singleton pregnancy; and
* parturients who were categorised as having an American Society of Anaesthesiologists (ASA) physical status
Exclusion Criteria:
* parturients with severe internal, surgical or obstetric comorbidities (including spinal deformities, hypertension, placental abruption, cholestasis in pregnancy, asthma, heart disease and abnormal coagulation parameters)
* parturients with a known allergy to the drugs used in this study
* parturients with severe mental illness who could not comply with doctors' instructions
* parturients with chronic pain syndrome, which is defined as pain that persists for a period longer than 3 months
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
32 Years
Study:
NCT05582135
Study Brief:
Protocol Section:
NCT05582135