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 @ 11:25 PM
Ignite Modification Date:
2025-12-24 @ 11:25 PM
NCT ID:
NCT02853656
Eligibility Criteria:
Inclusion criteria
* aged ≥ 18 years
* confirmed pregnancy
* gestational age between 22 and 34 weeks
* self-reported signs, symptoms or complaints suggestive of preterm labour;
* abdominal pain
* contractions
* pelvic pressure
Exclusion criteria
* unable to provide written informed consent
* multiple pregnancy
* participating in an interventional clinical trial
* a symptom not associated with idiopathic threatened preterm delivery (e.g. trauma)
* contraindicated to either fFN or PhIGFBP-1; e.g.
* vaginal bleeding
* cervical dilation ≥3cm dilated
* evidence of rupture of membranes
* had intercourse in last 24 hours
* cervical cerclage in situ
* placenta praevia
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT02853656
Study Brief:
Protocol Section:
NCT02853656