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 @ 2:31 AM
Ignite Modification Date:
2025-12-25 @ 2:31 AM
NCT ID:
NCT05586334
Eligibility Criteria:
Inclusion Criteria:
* Pregnant with live fetus(es)
* Emergency room visit between 22 and 34 days of pregnancy + 6 days
* For a suspicion of PTL defined by :
* Uterine contractions (UC) objectified during the consultation (questioning, clinical examination, external tocography),
* And/or clinical or ultrasound changes of the uterine cervix;
* OR for any other reason but with EC and/or clinical or ultrasound changes of the cervix on clinical examination
* Social security coverage or AME: patients receiving AME are at higher risk of PAD and preterm delivery.
* Signature of consent
Exclusion Criteria
* Age \< 18 years;
* Premature rupture of membranes
* Patient in labor with imminent delivery.
* Total absence of social care
* Minor or protected adult (guardianship or curatorship)
* Persons who do not speak French and not accompanied by a French-speaking third party
* Multiple pregnancy \>= 3
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT05586334
Study Brief:
Protocol Section:
NCT05586334