New Tool to Predict Risk of Spontaneous Preterm Birth in Asymptomatic High-risk Women
试验速览
- 阶段
- 不适用
- 入组人数
- 258
- 试验地点
- 2
- 主要终点
- Spontaneous preterm birth before 34.0 and 37.0 weeks of gestation
研究概览
简要总结
The QUIPP tool integrates information of obstetrical history, quantitative fetal fibronectin (qfFN) and cervical length to predict the risk of sPTB in asymptomatic high-risk women.
The aim of this study is to evaluate the QUIPP tool in our setting in order to optimize the management of women at high risk for sPTB and to validate in a randomized clinical trial, whether the use of QUIPP improves efficiently the management of our asymptomatic high-risk women when it is compared with the current clinical management.
Design: Randomized controlled trial. Inclusion criteria: Asymptomatic singleton pregnancies 18,0-22,6 weeks at high-risk for sPTB. Sample size: According to a non-inferiority analysis, 129 pregnant women will be needed for each arm.
Methodology: Patient selection and who consent to participate in the study will be randomized into two arms: a) Intervention group: QUIPP tool will be used to select and manage patients attending our PBPC: high-risk patients will be followed-up in our PBPC and low-risk patients will be discharged from PBPC and managed in a low-risk unit. b) Control group: Women will be managed according to current clinical practice.
Main Outcome: sPTB <34,0 and <37,0 weeks of gestation. Secondary Outcomes: Pregnancy outcomes and a neonatal composite morbidity. Expected Results: Perinatal outcomes are similar in the intervention and control group although the intervention group using the QUIPP tool required less medical resources.
详细描述
Preterm birth (PTB) is a leading cause of perinatal morbidity and mortality. Women at high-risk of preterm birth are those with a previous spontaneous preterm birth (sPTB) or preterm premature rupture of membranes before 35 weeks of gestation, uterine malformation, surgery on uterine cervix or a short cervical length; these women have a global risk of PTB about 30% but still 75%-85% of these women will deliver at term without any intervention.
The availability of a specialized Preterm Birth Prevention Clinic (PBPC) is relevant for the management of these high-risk pregnant women and it results in a reduction in the risk of recurrent sPTB, pregnancy prolongation and a reduction in the rate of major neonatal morbidity. However, it implies higher outpatient care costs as well as trained personnel and intensive follow-up management even for those women not destined to deliver preterm QUIPP is a free smartphone application that integrates the obstetrical history of high-risk women, the cervical length and the value of quantitative fetal fibronectin to predict the risk of preterm birth. QUIPP will determinate the risk of preterm birth in these high-risk women.
Patients will be randomized in two groups: Intervention group (QUIPP tool arm): QUIPP tool is applied and patients with a high-risk result will be follow-up in a high-risk unit (PBPC) and patients with a low-risk value will be managed in a low-risk unit. Control group (no QUIPP tool arm): current management in a PBPC will be applied.
The use of QUIPP will allow determining which asymptomatic pregnancies with risk factors for sPTB will deliver preterm. Furthermore, we expect to provide the non-specialized clinician with an objective, useful, accurate and efficient tool to manage these women with same pregnancy and neonatal outcomes and using less resource.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Diagnostic
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Age ≥ 18 years old
- •Asymptomatic singleton pregnancies, with at least one of the following: Previous spontaneous preterm delivery or a preterm premature rupture of membranes ≤ 346 weeks of gestation, Previous spontaneous second trimester miscarriage, Previous surgery on uterine cervix, Incidental finding of cervical length less than 25mm, Uterine malformations.
- •Able to sign informed consent form.
排除标准
- •Multiple pregnancies.
- •Congenital, chromosomal abnormalities or stillbirth in current pregnancy.
- •No patient consent to participate in the study
- •Women with an obstetrical history of iatrogenic preterm birth indicated for maternal or fetal conditions.
- •Symptomatic high-risk women or preterm prelabor rupture of membranes in current pregnancy.
- •Pregnant women with an indication of prophylactic cervical cerclage due to her own obstetrical history.
- •Pregnant women with a short cervix detected by ultrasound and with an indication to perform a cervical cerclage, prior to study inclusion.
研究组 & 干预措施
Intervention group: QUIPP tool arm
In this group, QUIPP tool will be used to select and manage patients attending our PBPC: high-risk patients will be followed-up in our PBPC and low-risk patients will be discharged from PBPC and managed in a low-risk unit.
干预措施: QUIPP (Device)
Control group: no QUIPP tool arm
Women will be managed according to current clinical practice.
结局指标
主要结局
Spontaneous preterm birth before 34.0 and 37.0 weeks of gestation
时间窗: 3.5 years
Delivery \< 34.0 and \<37.0 weeks of gestation ( Yes/No )
次要结局
- Clinical chorioamnionitis(3.5 years)
- 5 min APGAR score <7(3.5 years)
- Hospital admission due to sPTB or PPROM(3.5 years)
- Maternal mortality(3.5 years)
- umbilical artery pH at delivery <7.1(3.5 years)
- NCIU admission(3.5 years)
- Respiratory distress syndrome(3.5 years)
- Neonatal sepsis(3.5 years)
- Neonatal mortality(3.5 years)
- Emergency department visits due to uterine contractions(3.5 years)
- Gestational age at delivery(3,5 years)
- Intraventricular haemorrhage(3.5 years)
- Necrotizing enterocolitis(3.5 years)
- Need for respiratory support(3.5 years)
研究者
Montse Palacio
Medical Doctor. Physician Doctor. Senior consultant
Hospital Clinic of Barcelona