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