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 @ 2:43 AM
Ignite Modification Date:
2025-12-25 @ 2:43 AM
NCT ID:
NCT07264933
Eligibility Criteria:
Inclusion Criteria:
* primigravida with a gestational age of ≥37 weeks
* express a desire for postpartum contraception.
* acceptance to participate and to provide written informed consent
* willing to attend follow-up for 6 months postpartum.
Exclusion Criteria:
* Known uterine anomalies
* Chorioamnionitis
* Premature rupture of membranes \> 24 hours
* Previous uterine surgery
* Cervical dysplasia
* Uterine fibroids
* Multiple gestation
* Placenta previa or placental abruption
* Preeclampsia or eclampsia
* Hemoglobin \< 10 g/dL
* Any uncontrolled systemic disease
* Current tobacco use
* Chronic corticosteroid therapy
* Inability to provide informed consent
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT07264933
Study Brief:
Protocol Section:
NCT07264933