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临床试验/NCT05968794
NCT05968794招募中不适用

The Effectiveness of Cerclage for the Reduction of Extreme Preterm Birth and Perinatal Mortality in Twin Pregnancies With a Short Cervix or Dilatation

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)13 个研究点 分布在 2 个国家目标入组 238 人开始时间: 2023年5月15日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
238
试验地点
13
主要终点
Rate of extreme preterm birth

研究概览

简要总结

The goal of this clinical trial is to assess the effectiveness of a cerclage in women with a twin pregnancy with a midpregnancy short cervix or cervical dilatation compared to standard treatment (no cerclage) in the prevention of extreme preterm birth < 28 weeks of gestational age.

The main question it aims to answer is: What is the effectiveness of a cerclage in women with a twin pregnancy with a midpregnancy short cervix or cervical dilatation compared to standard treatment (no cerclage) in the prevention of extreme preterm birth < 28 weeks of gestational age?

Participants will be randomly assigned to the intervention (cerclage) or comparison (no cerclage) group.

详细描述

Rationale: In the Netherlands, 250 women with a twin pregnancy deliver at < 28 weeks per year, resulting in 157 perinatal deaths. A vaginal cerclage could be an effective surgical method to reduce cervical insufficiency and with that preterm birth, but the evidence regarding its effectiveness on extreme preterm birth and (long term) neonatal outcome is lacking.

Objective

To assess the effectiveness of a cerclage in women with a twin pregnancy with a midpregnancy short cervix or cervical dilatation compared to standard treatment (no cerclage) in the prevention of extreme preterm birth < 28 weeks of gestational age.

Nature and extent of the burden and risks associated with participation, benefit and group relatedness: A vaginal cerclage is a minor and safe surgical procedure commonly performed in singleton pregnancies with a short cervix and a previous preterm birth in all the participating centers, thus there is experience in the participating hospitals. The results of this study will show whether a vaginal cerclage reduces extreme preterm birth in women with twin pregnancy and a short cervix, and its accompanying perinatal complications. If proven effective, the implementation of this intervention will have a huge impact on the lifelong health of these children and their families.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

盲法说明

Participants and investigators will not be blinded for the intervention.

入排标准

年龄范围
16 Years 至 —(Child, Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Women (> 16 years of age) with a twin pregnancy and:
  • an asymptomatic short cervix at routine ultrasound investigation (below 24 weeks of gestation) OR
  • cervical dilatation (below 24 weeks of gestation)

排除标准

  • Women with a mono-amniotic twin pregnancy
  • Women with twin pregnancy in which one or both children are diagnosed with a major structural, congenital or chromosomal abnormality that is likely to influence the composite adverse neonatal outcome.
  • Women with dilatation of the cervix and signs of clinical intra-uterine infection, defined by the presence of fever ≥ 38 degrees Celsius.
  • Women with overt symptoms of preterm labour at time of measurement of short cervix (regular contractions, PPROM, recurrent blood loss).
  • Women with a placenta previa, defined as a placenta position covering the internal ostium of the cervix.
  • Women who do not master the Dutch of English language and therefore not able to give written consent

结局指标

主要结局

Rate of extreme preterm birth

时间窗: <28 weeks of gestation

次要结局

  • Days in NICU(Up to 3 months corrected age)
  • Rate of maternal outcomes(Up to 3 months corrected age)
  • Number of neonates with bronchopulmonary dysplasia(Up to 3 months corrected age)
  • Number of neonates with periventricular leucomalacia > grade 1(Up to 3 months corrected age)
  • Number of neonates with intraventricular hemorrhage > grade 2(Up to 3 months corrected age)
  • Days on ventilation support(Up to 3 months corrected age)
  • Rate of Premature rupture of membranes(Up to 42 weeks of pregnancy)
  • Gestational age at delivery(At delivery)
  • Rate of Preterm birth(<24, <32, <34 and <37 weeks)
  • Adverse neonatal outcome(Up to 3 months corrected age)
  • Number of neonates with necrotizing enterocolitis > stage 2(Up to 3 months corrected age)
  • Number of neonates with proven sepsis(Up to 3 months corrected age)
  • Maternal quality of life assessed by the 'European Quality of life 5-Dimension 5-Level' score(Up to 3 months corrected age)
  • Number of neonates with retinopathy of prematurity > stage 2(Up to 3 months corrected age)
  • Perinatal death(Up to 3 months corrected age)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Martijn A. Oudijk, MD, PhD

Prof.dr.

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

研究点 (13)

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