C-Stich

Cerclage Suture Type for an Insufficient Cervix and its effect on Health (C-STICH)

THE MAIN TRIAL FEATURES:

  • A multi-centre randomised controlled trial covering obstetrics and gynaecology centres nationwide.
  • Funded by the National Institute for Health Research Health Technology Assessment Programme (NIHR HTA).
  • Run by Mr Philip Toozs-Hobson (Chief Investigator).
  • Birmingham Clinical Trials Unit at the University of Birmingham are overseeing the administrative aspects of the Trial.
  • The target recruitment is 900 patients by September 2017.
  • Participating women will be randomly allocated to either a monofilament or braded suture.
  • The primary objective is to examine the effect of using a monofilament suture material compared with a braided suture material on pregnancy loss rate (defined as miscarriage, stillbirth, neonatal death in the first week of life) and neonatal mortality up to 7 days post-delivery in women presenting with an insufficient cervix and treated with cervical cerclage.

For the Trial Schema click here