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 @ 2:38 AM
Ignite Modification Date:
2025-12-25 @ 2:38 AM
NCT ID:
NCT01937234
Eligibility Criteria:
Inclusion Criteria:
* Primigravida
* Singleton pregnancy
* Term gestation i.e. 37- 42 weeks
* Sure reliable dates
* Vertex presentation, occipitoanterior position
* Spontaneous onset of labor
* Regular uterine contractions at every 5 min ,each lasting for 20 sec
* Cervical dilatation of 3-5cm
* With or without rupture of membranes
* No evidence of maternal or fetal distress
Exclusion Criteria:
* Mal-presentations
* Mal-positions
* Multifetal pregnancy
* Cephalopelvic disproportion
* history of cervical surgery or injury
* Hypersensitivity to metoclopramide
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
35 Years
Study:
NCT01937234
Study Brief:
Protocol Section:
NCT01937234