Predictive test for preterm birth in threatened preterm labor
Official title: Evaluation of a New Predictive Test of Preterm Birth in Case of Threatened Preterm Labor
Run by University Hospital, Strasbourg, France · NCT04374916 · Data updated 2026-11-12
A test called Premaquick is being tried to see if it can better predict preterm delivery in pregnant people with threatened preterm labor.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 200 (estimated) |
| Sponsor | University Hospital, Strasbourg, France Academic / other |
| Locations | 1 site (Strasbourg) |
| Status | Recruiting |
| Started | August 11, 2020 |
| Main results expected | April 4, 2025 |
| Study ends | September 2026 |
| Registry record updated | August 21, 2026 |
| Trial ID | NCT04374916 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults over 18 with singleton pregnancies between 24 and 33+6 weeks, experiencing threatened preterm labor, and who are affiliated with a social security health regime.
✕Probably not a fit
Women not at elevated risk according to the test results or whose labor spontaneously progresses may not receive a direct benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study compares the Premaquick test with the PARTOSURE test to predict preterm delivery in women with threatened preterm labor between 24 and 33+6 weeks of gestation. It is an interventional investigation evaluating prognosis-based testing rather than a treatment. Eligible participants are adults with singleton pregnancies and recent uterine contractions, who meet specific ultrasound and clinical criteria. The study is led by University Hospital Strasbourg, with recruitment at Hôpitaux Universitaires de Strasbourg, and uses the two biomarker-based tests to inform risk of preterm birth. Results could guide clinical decisions and management in threatened preterm labor cases.
Why it matters
Potential benefit: If successful, the test could help clinicians identify women at higher risk for preterm birth and tailor interventions accordingly.
How similar studies have gone: Previous studies have explored biomarker-based tests for predicting preterm birth, but direct head-to-head evidence comparing Premaquick with PARTOSURE is limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patient aged \> 18 years (with no upper age limit) * Patient affiliated to a social security health regime * Between 24 and 33 + 6 weeks of gestation (amenorrhea) * Singleton pregnancy * Patient with a TPL: Uterine contractions during the last 24 hours felt by the patient, painful or not, and cervix less than or equal to 25 mm on endovaginal ultrasound * Having signed an informed consent form Exclusion Criteria: * Twin pregnancy * Sexual intercourse less than 24 hours from inclusion * Cervical cerclage * Abundant metrorrhagia * Premature rupture of membranes * Pre-eclampsia * Congenital malformation * Presence of a placenta previa * Pelvic examination in the previous 24 hours (compared to inclusion) * Patient under guardianship, curatorship or safeguard of justice * Persons deprived of their liberty by judicial or administrative decision * Persons under psychiatric care under duress
Where it's running
-
Hôpitaux Universitaires de Strasbourg
Strasbourg, France Recruiting
Study contacts
- Study coordinator: Antoine KOCH, PHD
- Email: antoine.koch@chru-strabourg.fr
- Phone: +33 3 88 12 75 03
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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PremaSure: a self-test to check the risk of preterm delivery in symptomatic pregnant patients.
This will test whether the PremaSure self-test can tell symptomatic pregnant patients if they are likely to deliver within 7 or 14 days.
-
Higher-dose versus standard-dose aspirin to prevent another early preterm birth
This trial tests whether taking 162 mg daily aspirin instead of 81 mg, starting at 10–15 weeks of pregnancy, helps people with a prior early preterm birth avoid another preterm delivery or fetal death before 35 weeks.
-
Evaluating a device to predict preterm birth risk in pregnant women
This study is testing a new device to see if it can help predict the risk of preterm birth in pregnant women who are having early labor symptoms.
-
Monitoring blood glucose in pregnant women receiving betamethasone for fetal lung development
This study looks at how the medication betamethasone affects blood sugar levels in pregnant women who don't have diabetes but are at risk of preterm birth.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.