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Study identifier: NCT07637318 Synced from ClinicalTrials.gov · August 04, 2026
● Not Yet Recruiting

Prediction of Labor Induction Outcome in Nulliparous Women

Condition: Nulliparous Patient With Unfavourable Cervix, Undergoing Labor Induction at Term ≥ 39SA  ·  Sponsor: Assistance Publique - Hôpitaux de Paris

PhaseN/A
Planned participants190
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

Labor induction rates are increasing worldwide, yet nulliparous patients remain at high risk of failed induction and intrapartum cesarean delivery as well as prolonged labor which are associated with increased maternal morbidity, adverse outcomes in future pregnancies, increased neonatal morbidity and negative childbirth experience. This study aims to evaluate whether macrophage activation biomarkers in cervicovaginal secretions can predict successful labor induction in low-risk nulliparous women at term with an unfavorable cervix (Bishop score \<6). The study focuses on three patented biomarkers of "imminence of delivery" (MCP1, CD14, and CD163), previously shown to be markedly elevated during spontaneous labor. We hypothesize that higher biomarker concentrations reflect biological readiness for labor and are associated with successful induction, defined as entry into the active phase of labor (cervical dilation ≥6 cm). Secondary objectives include evaluating the association between biomarker concentrations and labor progression. Identifying reliable predictive biomarkers could improve patient selection for induction and optimize obstetrical management in nulliparous women.

This description comes directly from the study's public registry record.

Talk to the study team

Maëlys NKOBETCHOU, Medical Degree  ·  01 58 41 38 18  ·  maelys.nkobetchou@aphp.fr

Christelle AUGER  ·  01 71 76 07 53  ·  christelle.auger@aphp.fr

Always discuss trial participation with your own doctor first.

Locations (1)

AP-HP - Hôpital Cochin - Maternité Port-RoyalParis, Île-de-France Region, France

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