Edinburgh Clinical Trials


Cervical Ripening at Home or In-Hospital – prospective cohort study and process evaluation

Our aim is to compare home versus in-hospital cervical ripening to determine whether home cervical ripening is within an acceptable margin of in-hospital cervical ripening for the safety outcome of neonatal unit (NNU) admission, whether it is more acceptable to women and whether it is cost-effective from both NHS and patient perspectives.    


Chief Investigator:  Dr Sarah Stock 


Number and location of participating sites / geographical scope (by region/ country):  Expected 30 sites (no sites open yet)

EudraCT number: N/A

ISRCTN number: N/A


Funder:  NIHR HTA  

Start and End date

Of grant award: 01/12/2019 - 30/11/2022

Of recruitment: Not yet open to recruitment  


Current status: In set up  

Website: TBC  

Email: CHOICE.Study@ed.ac.uk


 GDPR Privacy Statement: If you have participated in this study and would like to read how it complies with GDPR, please read this document.


Chief Investigator: 

Dr Sarah Stock, Usher Institute of Population Health Sciences and Informatics, NINE Edinburgh BioQuarter, 9 Little France Road, Edinburgh, EH16 4UX   


Trial Manager: Fiona Wee, 0131 651 9909


ECTU Involvement:  Trial Management, Statistics, Data Management