Study protocol for two randomised controlled trials evaluating the effects of Cerclage in the reduction of extreme preterm birth and perinatal mortality in twin pregnancies with a short cervix or dilatation: the TWIN Cerclage studies.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
10 May 2024
Historique:
medline: 11 5 2024
pubmed: 11 5 2024
entrez: 10 5 2024
Statut: epublish

Résumé

Twin pregnancies have a high risk of extreme preterm birth (PTB) at less than 28 weeks of gestation, which is associated with increased risk of neonatal morbidity and mortality. Currently there is a lack of effective treatments for women with a twin pregnancy and a short cervix or cervical dilatation. A possible effective surgical method to reduce extreme PTB in twin pregnancies with an asymptomatic short cervix or dilatation at midpregnancy is the placement of a vaginal cerclage. We designed two multicentre randomised trials involving eight hospitals in the Netherlands (sites in other countries may be added at a later date). Women older than 16 years with a twin pregnancy at <24 weeks of gestation and an asymptomatic short cervix of ≤25 mm or cervical dilatation will be randomly allocated (1:1) to both trials on vaginal cerclage and standard treatment according to the current Dutch Society of Obstetrics and Gynaecology guideline (no cerclage). Permuted blocks sized 2 and 4 will be used to minimise the risk of disbalance. The primary outcome measure is PTB of <28 weeks. Analyses will be by intention to treat. The first trial is to demonstrate a risk reduction from 25% to 10% in the short cervix group, for which 194 patients need to be recruited. The second trial is to demonstrate a risk reduction from 80% to 35% in the dilatation group and will recruit 44 women. A cost-effectiveness analysis will be performed from a societal perspective. This study has been approved by the Research Ethics Committees in the Netherlands on 3/30/2023. Participants will be required to sign an informed consent form. The results will be presented at conferences and published in a peer-reviewed journal. Participants will be informed about the results. ClinicalTrials.gov, NCT05968794.

Identifiants

pubmed: 38729756
pii: bmjopen-2023-081561
doi: 10.1136/bmjopen-2023-081561
doi:

Banques de données

ClinicalTrials.gov
['NCT05968794']

Types de publication

Journal Article Clinical Trial Protocol Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e081561

Informations de copyright

© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Lissa van Gils (L)

Department of Obstetrics and Gynaecology, Amsterdam UMC, Amsterdam, The Netherlands L.vangils1@amsterdamumc.nl.

Marjon A de Boer (MA)

Department of Obstetrics and Gynaecology, Amsterdam UMC, Amsterdam, The Netherlands.

Judith Bosmans (J)

Department of Health Sciences, Amsterdam UMC Location AMC, Amsterdam, Noord-Holland, The Netherlands.

Ruben Duijnhoven (R)

Department of Obstetrics and Gynaecology, Amsterdam UMC, Amsterdam, The Netherlands.

Sam Schoenmakers (S)

Department of Obstetrics and Gynaecology, Erasmus Medical Center, Rotterdam, The Netherlands.

Jan B Derks (JB)

Department of Obstetrics, University Medical Centre Utrecht, Utrecht, The Netherlands.

Jelmer R Prins (JR)

Department of Obstetrics and Gynaecology, University Medical Center Groningen, Groningen, The Netherlands.

Salwan Al-Nasiry (S)

Department of Obstetrics and Gynaecology, Maastricht UMC+, Maastricht, The Netherlands.

Margo Lutke Holzik (M)

Department of Obstetrics and Gynecology, Leiden Universitair Medisch Centrum, Leiden, The Netherlands.

Enrico Lopriore (E)

Department of Neonatology and Fetal Medicine, Leiden University Medical Center, Leiden, The Netherlands.

Joris van Drongelen (J)

Department of Obstetrics and Gynecology, Radboud Universiteit, Nijmegen, The Netherlands.

Marieke H Knol (MH)

Department of Obstetrics and Gynaecology, Isala Zwolle, Zwolle, The Netherlands.

Judith O E H van Laar (JOEH)

Department of Obstetrics & Gynaecology, Máxima Medical Center, Veldhoven, The Netherlands.

Yves Jacquemyn (Y)

University Hospital Antwerp, Antwerpen, Belgium.

Caroline van Holsbeke (C)

AZ Sint-Lucas Brugge, Brugge, West-Vlaanderen, Belgium.

Isabelle Dehaene (I)

University Hospital Ghent, Gent, Belgium.

Liesbeth Lewi (L)

Fetal Medicine Unit, KU Leuven University Hospitals Leuven, Leuven, Flanders, Belgium.

Hannes van der Merwe (H)

Fetal Medicine Unit, KU Leuven University Hospitals Leuven, Leuven, Flanders, Belgium.

Wilfried Gyselaers (W)

Department of Obstetrics and Gynecology, Hospital Oost-Limburg, Genk, Belgium.

Sylvia A Obermann-Borst (SA)

Care4Neo, Neonatal patient and parent advocacy organization, Rotterdam, The Netherlands.

Mayella Holthuis (M)

Patient organization 'Extreme Vroeggeboorte', Amsterdam, The Netherlands.

Ben W Mol (BW)

department of obstetrics and gynaecology, school of medicine, Monash University, Melbourne, Victoria, Australia.

Eva Pajkrt (E)

Department of Obstetrics and Gynaecology, Amsterdam UMC, Amsterdam, The Netherlands.

Martijn A Oudijk (MA)

Department of Obstetrics and Gynaecology, Amsterdam UMC, Amsterdam, The Netherlands.

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