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 @ 4:27 AM
Ignite Modification Date:
2025-12-25 @ 4:27 AM
NCT ID:
NCT04969120
Eligibility Criteria:
Inclusion Criteria:
* primigravida
* singleton pregnancy
* termgestation (37-42 weeks)
* sure reliable dated
* vertex presentation , occipito-anterior position
* regular uterine contractions at every 5 minutes,each lasting for 20 seconds
* cervical dilatation of 5 cm
* with or without rupture of membrane
* no evidence of maternal or fetal distress
Exclusion Criteria:
* chorioamnionitis
* scarred uterus e.g. myomectomy
* cephalopelvic dispropotion
* history of cervical surgery or injury
* hypersensitivity to metoclopramide
Healthy Volunteers:
True
Sex:
FEMALE
Study:
NCT04969120
Study Brief:
Protocol Section:
NCT04969120