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Completed

NCT Number: NCT03073317

PREPARE, Prematurity Reduction by Pre-eclampsia Care

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.

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Key information

Age range

10 year–50 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Hospital de Clinicas de Porto Alegre, Porto Alegre, RIO GDE DO SUL, Brazil

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About this study

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).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • pregnancy before 16 weeks
  • delivery at designed maternity center

Exclusion criteria

  • not viable fetus

Treatment and study plan

FullPIERS and sFlit/PLGF (Soluble fms-Like Tyrosine Kinase-1-to-Placental Growth Factor Ratio)

Diagnostic Test

Once the centre is randomised to receive the intervention, all eligible women will have serum sFlt1/PlGF measurement performed and fullPIERS assessment and both results will be revealed to the care providers. This will include all women with pre-eclampsia or suspected pre-eclampsia cared for at the main hospital centres (and not be limited to women referred to the hospital from the community health centres). sFlt-1/PlGF will be tested by immunoassays (Roche Platform®). The result read out is provided by specific machines provided by Roche in less than one hour, which permits rapid clinical decision-making. Risk stratification using fullPIERS will be performed on tablet computers using a pre-defined risk scoring system integrated within the MedSciNet database.

Primary outcomes

  1. patients with preterm preeclampsia

    Time frame: 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

Secondary outcomes

  1. proportion of women delivered in the centers who delivered prematurely

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

    proportion of women delivered with preterm pre-eclampsia/ total deliveries for pre-eclampsia, where preterm is <37 weeks' gestation

  2. proportion of women delivered in the centres with preterm pre-eclampsia

    Time frame: 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 <34 weeks' gestation

  3. RATE PRETERM PRE-ECLAMPSIA DELIVERIES

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

    proportion of women delivered with preterm pre-eclampsia/ total deliveries for pre-eclampsia, where preterm is <34 weeks' gestation

  4. maternal morbidity and mortality defined as a composite of maternal mortality and features of 4a-4f

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

    4a. HELLP syndrome cases of HELLP syndrome in women with pre-eclampsia

    4b. pulmonary oedema cases of pulmonary oedema in women with pre-eclampsia

    4c. eclampsia proportion of women with eclampsia

    4d. cerebrovascular accident (CVA) cases of maternal cerebrovascular accident (stroke or coma) in women with pre-eclampsia

    4e. renal dysfunction cases of renal dysfunction in women with pre-eclampsia, where criteria is serum creatinine of >150

  5. frequency of severe hypertension

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

    systolic BP ≥ 160 mmHg or diastolic BP ≥ 110 mm/Hg

  6. placental abruption

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

    cases of placental abruption

  7. mode of delivery (total C-sections)

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

    total number of reported C-sections

  8. stillbirth

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

    cases of stillbirth at >20 weeks

  9. early neonatal mortality

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

    cases of neonatal mortality at <7 days

  10. admission to the neonatal care unit

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

    cases of admission to the neonatal care unit due to prematurity related to pre-eclampsia

Sponsors and collaborators

Lead sponsor

Instituto Fernandes Figueira

Other Gov

Collaborators

  • CoLab
  • HGA
  • HOSPITAL MATERNIDADE LEONOR MENDES DE BARROS
  • Hospital de Clinicas de Porto Alegre
  • SMSDC/RJ
  • UPECLIN HC FM Botucatu Unesp
  • University of Campinas, Brazil

Registry information

Acronym: PREPARE

Important dates

Study start
2016
Primary completion
2019
Study completion
2020
First posted
Mar 8, 2017
Registry last updated
Jul 18, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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