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Study identifier: NCT06122506 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Nordic Randomized Trial on Laparoscopic Versus Vaginal Cerclage

Condition: Preterm Birth · Cervical Insufficiency  ·  Sponsor: University of Aarhus

PhaseNA
Planned participants188
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

Every year 15 million babies are born prematurely, which can lead to death or life-long disabilities. It is often caused by a dysfunction of the uterine cervix, which constitutes the narrow channel between the vagina and womb. During pregnancy, this channel must remain closed until the beginning of term labor. A weak cervix may not withstand the weight of the fetus, the amniotic fluid and the placenta and the cervical canal will open and cause late miscarriage or preterm delivery. To prevent this, a band (cerclage) can be applied around the cervix either vaginally or laparoscopically prior to a new pregnancy. To evaluate which treatment is best for most women, we will randomize (allocate by chance) women at risk for preterm birth, to either vaginal cerclage or laparoscopic cerclage in the Nordic countries and England

This description comes directly from the study's public registry record.

Talk to the study team

Lea K Hansen, MD  ·  +45 51910993  ·  lea.hansen@clin.au.dk

Always discuss trial participation with your own doctor first.

Locations (2)

Aarhus University HospitalAarhus N, DenmarkRecruiting
RigshospitaletCopenhagen, DenmarkRecruiting

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Source record: clinicaltrials.gov/study/NCT06122506