A novel aspiration technique to assess cervical remodelling in patients with or without cervical shortening: Sequence of first changes, definition of cut-off values and impact of cervical pessary, stratified for cervical length

PLoS One. 2023 Apr 6;18(4):e0283944. doi: 10.1371/journal.pone.0283944. eCollection 2023.

Abstract

Background: The therapeutic significance of the cervical pessary has been confirmed by several studies. However, the underlying mechanism by which pessaries reduce the risk of a preterm birth remains elusive. The aim of this study is to investigate the hypothesis whether the application of a cervical pessary may stabilize the ectocervical stiffness in order to achieve a cervical arrest.

Methods: This is a prospective, controlled, non-interventional, post-market, monocentric, longitudinal, cohort study in a tertiary maternity hospital to determine ectocervical stiffness and its changes measured before and after placement of a pessary in singleton pregnancies with cervical shortening in the mid trimester. In order to assess reference values for cervical stiffness, we measured also singleton pregnancies with normal cervical length in the same gestational week spectrum. The cervical stiffness measured with the Pregnolia System as the Cervical Stiffness Index (CSI, in mbar) shall be the primary endpoint, whilst patient delivery data (gestational age, mode of delivery and complications) will be the secondary endpoint. In this pilot study, up to 142 subjects will be enrolled to have a total of 120 subjects (estimated dropout rate of 15%) to complete the study; pessary cohort: 60 (up to 71 recruited), control group: 60 (up to 71 recruited).

Discussion: Our hypothesis is that patients with cervical shortening will present with lower CSI values and that pessary placement will be able to stabilize the CSI values through further prevention of cervical remodelling. The measurement of controls with normal cervical length shall serve as a reference.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cervix Uteri / diagnostic imaging
  • Cohort Studies
  • Female
  • Humans
  • Infant, Newborn
  • Pessaries / adverse effects
  • Pilot Projects
  • Pregnancy
  • Premature Birth* / etiology
  • Prospective Studies
  • Uterine Cervical Incompetence*

Grants and funding

This study is supported by Asklepios Kliniken Hamburg GmbH, represented by ASKLEPIOS Proresearch. The funder had no role in the design of the study, the collection, analysis, and interpretation of data and in writing the manuscript. Pregnolia AG (www.pregnolia.com) provides the devices for this study and a grant to support the study.