Clinical trial Recruiting at 1 site Interventional Ages 18 and up Women only

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 typeInterventional
Ages18 Years and up
SexWomen only
Enrollment200 (estimated)
SponsorUniversity Hospital, Strasbourg, France
Academic / other
Locations1 site (Strasbourg)
StatusRecruiting
StartedAugust 11, 2020
Main results expectedApril 4, 2025
Study endsSeptember 2026
Registry record updatedAugust 21, 2026
Trial IDNCT04374916 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

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.