This study aims to determine whether the Arabin cervical pessary prevents preterm birth in women with a twin pregnancy and a short cervix.
STOPPIT-2 is a multicentre open label randomised controlled trial of the Arabin pessary (CE marked Device) versus Standard treatment in women with twin pregnancy. The study is in two phases - a SCREENING phase, in which women with a short cervix (cervical length of ( less or equal to 35mm) will be identified, and a TREATMENT phase, in which women with a short cervix will be randomised to treatment with Arabin pessary or Standard treatment. Women will be seen in the antenatal clinic setting. An internal pilot phase will take place, with ten interviews being conducted with pregnant women to explore the acceptability of proposed methods of recruitment, their information requirements, their views of the consent and randomisation processes, and the delivery of the intervention, including the screening component. The interviews will also explore their understanding and expectations of trial participation. The findings of this pilot phase will feed into the next phase of the trial and support the design of the interview guides for the main nested qualitative study. This pilot phase is separate from the main study. Later on we will ask both women and healthcare professionals about their experiences of the study, via questionnaires and face-to-face interviews.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
2,228
The Arabin pessary is CE-certified for preventing Spontaneous Preterm Birth (SPB) (CE 0482 / EN ISO 13485: 2003 annex III of the council directive 93/42 EEC) and is being used in this study as per the CE certification and manufacturer's guidance.
The Arabin cervical pessary reduces spontaneous preterm labour leading to preterm birth
Gestation at delivery
Time frame: Delivery of the babies
Neonatal Outcomes
The investigators will collect a number of measures to ascertain neonatal well being.
Time frame: within 4 weeks after expected date of delivery
The profile of cervical length measurements in women with twin pregnancy in the UK
Cervical length
Time frame: 18-20 weeks gestation
Participant Satisfaction
Acceptability questionnaire
Time frame: 36 weeks gestation
Health economics
cumulative hospital costs
Time frame: 18-20 weeks gestation until 4 weeks postnatal
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
UZ Leuven
Leuven, Belgium
Countess of Chester
Chester, Cheshire, United Kingdom
St Mary's Hospital
Manchester, Cheshire, United Kingdom
Chesterfield Royal Hospital
Chesterfield, Derbyshire, United Kingdom
Derriford Hospital
Plymouth, Devon, United Kingdom
Poole Hospital
Poole, Dorset, United Kingdom
Basildon hospital
Basildon, Essex, United Kingdom
Hillingdon Hospital
Uxbridge, Greater London, United Kingdom
Royal Bolton Hospital
Bolton, Lancashire, United Kingdom
Royal Preston Hospital
Preston, Lancashire, United Kingdom
...and 47 more locations