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临床试验/NCT03073317
NCT03073317已完成不适用

PREPARE, Prematurity Reduction by Pre-eclampsia Care

Instituto Fernandes Figueira16 个研究点 分布在 1 个国家目标入组 1,250 人开始时间: 2016年12月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1,250
试验地点
16
主要终点
patients with preterm preeclampsia

研究概览

简要总结

Investigators will test a novel system of integrated care, to promote the use of the WORLD HEALTH ORGANIZATION Guidelines for the management of pre-eclampsia and initiate the use of a structured risk assessment strategy to reduce the incidence of preterm delivery from pre-eclampsia by providing obstetricians with the confidence to safely defer delivery of women with pre-eclampsia, identified to be of low risk.

详细描述

This proposal (PREPARE), led by Brazilian investigators in collaboration with the Global Pregnancy Collaboration (CoLab) is centred on 7 hospital centres and their 23 satellite community health centres (UBSs). There are two clinical initiatives: First, a programme of systematic knowledge transfer (KT) to encourage adoption of the WHO Guidelines to prevent pre-eclampsia as part of routine antenatal care (Objective 1); second an intervention to reduce unnecessary preterm deliveries for the management of pre-eclampsia. CoLab investigators have developed methods to identify those women with preterm pre-eclampsia whose pregnancies can be safely prolonged.4-6 In Objective 2.1, these methods will be applied to women presenting with definite or suspected pre-eclampsia at < 37 weeks' gestation. Investigators will determine the likelihood of an imminent adverse outcome in these women using Soluble fms-Like Tyrosine Kinase-1-to-Placental Growth Factor Ratio (sFlT-1/PlGF) measurement and fullPIERS clinical assessment. Prior studies with these approaches indicate more than 98% negative predictive value for adverse outcomes for both.4-6 Investigators will delay delivery in those whose risk is low, caring for patients in accordance with evidence-based WHO guidelines.Unlike medications, management cannot be tested in a blinded way. Management needs integrated skills and commitment from caregivers. Hence, a standard randomized controlled trial is inappropriate. Instead investigators propose a Stepped Wedge Design to study outcomes in the 7 geographically diverse study centres, throughout Brazil. At least 6 women with preterm pre-eclampsia will deliver at each centre every month. The primary outcome will be a lower rate of PRETERM BIRTH due to pre-eclampsia as a proportion of total deliveries in the centre(s) after implementation of the plan compared to prior to its introduction. The study will have 80% power to demonstrate a 25% reduction (2.0 - 1.5%). Investigators will assess maternal and foetal adverse events as secondary outcomes. Objective 2.2 will institute an intense program of knowledge transfer to implement the new management techniques. In Objectives 2.3 and 2.4 will determine patient and provider satisfaction and the economic impact of the care plan. In Objective 3 will establish a biobank and database to begin to assess demographic factors and biological analytes that may help identify unique predictive and diagnostic/pathophysiological features for pre-eclampsia in the Brazilian population (that may extend to other low and middle income countries (LMIC)). For two years at routine visits (≤16 weeks, 28-32 weeks) at each UBS, relevant data and plasma, serum, urine and DNA samples will be stored to the appropriate standards in the biorepository (at least 7000 cases). Investigators estimate that will acquire samples at delivery in at least 5000 of these women. For four years, biological samples from women with pre-eclampsia or other adverse outcomes and 2 matched controls will be collected at admission for labour (an additional 3,000 subjects). Objective 4 will initiate pilot studies to identify novel biomarkers, and compare these and other known pathophysiological factors with those from LMIC (Africa, India) and HIC using samples from CoLab. Additional funding will be sought for expansion and validation (e.g. Merck for Mothers). Investigators will also seek funding to address risk stratification in apparently low risk women, based on the samples collected at 28-32 weeks. Objective 5 will promote intellectual interactions and collaboration between the seven centres and CoLab. Ability to understand and cure complex adverse pregnancy outcomes leading to acute and long-range disability in children requires intensive collaboration across usual "silos" including hospitals and nations. The coordinators anticipate the interaction of investigators and care providers in the seven centres will foster intellectual collaboration and improved standardized care. Brazilian investigators will become members of CoLab, increasing its unique vision, expertise and resources (current data and biological materials from 28 centres). worldwide).

研究设计

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

入排标准

年龄范围
10 Years 至 50 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • pregnancy before 16 weeks
  • delivery at designed maternity center

排除标准

  • not viable fetus

结局指标

主要结局

patients with preterm preeclampsia

时间窗: researchers will be assessing and reporting outcome through month 1 to month 34 of the study

proportion of women delivered in the centres with preterm pre-eclampsia (deliveries with preterm pre-eclampsia/ total deliveries), where preterm is \<37 weeks' gestation

次要结局

  • proportion of women delivered in the centres with preterm pre-eclampsia(researchers will be assessing and reporting outcome through month 1 to month 34 of the study)
  • early neonatal mortality(researchers will be assessing and reporting outcome through month 1 to month 34 of the study)
  • admission to the neonatal care unit(researchers will be assessing and reporting outcome through month 1 to month 34 of the study)
  • stillbirth(researchers will be assessing and reporting outcome through month 1 to month 34 of the study)
  • frequency of severe hypertension(researchers will be assessing and reporting outcome through month 1 to month 34 of the study)
  • mode of delivery (total C-sections)(researchers will be assessing and reporting outcome through month 1 to month 34 of the study)
  • RATE PRETERM PRE-ECLAMPSIA DELIVERIES(researchers will be assessing and reporting outcome through month 1 to month 34 of the study)
  • maternal morbidity and mortality defined as a composite of maternal mortality and features of 4a-4f(researchers will be assessing and reporting outcome through month 1 to month 34 of the study)
  • proportion of women delivered in the centers who delivered prematurely(researchers will be assessing and reporting outcome through month 1 to month 34 of the study)
  • placental abruption(researchers will be assessing and reporting outcome through month 1 to month 34 of the study)

研究者

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

Marcos Augusto Bastos Dias

PhD

Instituto Fernandes Figueira

研究点 (16)

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