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Clinical Trials/NCT05034861
NCT05034861
Recruiting
Not Applicable

COmputerized CTG Self-MOnitoring Versus Standard Doppler Assessment in Late-onset FGR: Study Protocol for a Randomized Controlled Trial

Institute of Mother and Child, Warsaw, Poland1 site in 1 country150 target enrollmentDecember 13, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Fetal Growth Restriction
Sponsor
Institute of Mother and Child, Warsaw, Poland
Enrollment
150
Locations
1
Primary Endpoint
Neonatal Intensive Care Unit admission
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

Fetal growth restriction is one of the major causes of perinatal morbidity, mortality and adverse neurological outcome. Growth restricted fetuses do not reach their potential due to multiple factors. Although early (<32 weeks' gestation) FGR is associated with the highest risk of adverse outcomes, late FGR (≤ 32 weeks' gestation) is more common in daily maternal-fetal medicine care. Despite its' prevalence, optimal standard for monitoring differs between the centers and may be difficult in case of limited access to advanced perinatal care. We present a protocol for COmputerized CTG Self-MOnitoring versus Standard Doppler assessment in Late-onset FGR (COSMOS) trial, which is a prospective, cross-over, open-label and randomized trial that compares two different protocols for late-onset FGR observation.

All women carrying fetuses with late-onset FGR with positive end-diastolic flow in umbilical artery will be invited to participate in the randomized trial. Patients will be randomly divided into two groups: CTG - a group that will receive electronic device for cCTG home assessment, and Doppler - a group that will be monitored according to standard Doppler velocimetry criteria. Further management will depend on the arm of the study. Pregnancy and neonatal outcomes will be collected and analyzed.

Registry
clinicaltrials.gov
Start Date
December 13, 2022
End Date
December 2024
Last Updated
3 years ago
Study Type
Interventional
Study Design
Crossover
Sex
Female

Investigators

Sponsor
Institute of Mother and Child, Warsaw, Poland
Responsible Party
Principal Investigator
Principal Investigator

Urszula Nowacka

Principal Investigator

Institute of Mother and Child, Warsaw, Poland

Eligibility Criteria

Inclusion Criteria

  • women aged 18 years or older,
  • singleton pregnancy,
  • ≥32+0 and ≤36+6 weeks' of gestation,
  • fluent in Polish or English,
  • diagnosed with late-onset FGR based of the Delphi criteria,
  • with positive EDF in UA,
  • with macroscopically normal fetus on ultrasound assessment.

Exclusion Criteria

  • multiple pregnancy,
  • fetal malformations,
  • abnormal genetic testing results (if available),
  • uncertain pregnancy dating,
  • indication for immediate delivery within 48 hours after enrollment,
  • preterm prelabour rupture of membranes.

Outcomes

Primary Outcomes

Neonatal Intensive Care Unit admission

Time Frame: anytime after the recruitment visit or after delivery before discharge from the hospital or up to 6 weeks after delivery if discharged earlier

Incidence any admission to the Neonatal Intensive Care Unit

Condition at birth

Time Frame: 5 minutes after delivery

Incidence of Apgar score at 5 min \<7 or arterial pH of \<7.0 or venous \<7.1 or resuscitation (compressions, medications, intubation)

Respiratory distress syndrome

Time Frame: anytime after the recruitment visit or after delivery before discharge from the hospital or up to 6 weeks after delivery if discharged earlier

defined as need of surfactant and ventilation as a result of prematurity

Retinopathy

Time Frame: anytime after the recruitment visit or after delivery before discharge from the hospital or up to 6 weeks after delivery if discharged earlier

incidence of retinopathy requiring laser or anti-VEGF administration

Fetal/neonatal death

Time Frame: anytime after the recruitment visit or after delivery before discharge from the hospital or up to 4 weeks after delivery if discharged earlier

Rate of death in utero or after delivery before discharge from the hospital or up to 4 weeks after delivery if discharged earlier

Brain injury

Time Frame: anytime after the recruitment visit or after delivery before discharge from the hospital or up to 6 weeks after delivery if discharged earlier

Incidence of Intraventricular haemorrhage (IVH) grade II or above-defined as bleeding into the ventricles; or hypoxic-ischaemic encephalopathy or periventricular leukomalacia or seizures recorded by EEG

Ventilation

Time Frame: anytime after the recruitment visit or after delivery before discharge from the hospital or up to 6 weeks after delivery if discharged earlier

defined as need of positive pressure (continuous positive airway pressure (CPAP or nasal CPAP) or intubation rate

Cardiovascular support/treatment

Time Frame: anytime after the recruitment visit or after delivery before discharge from the hospital or up to 6 weeks after delivery if discharged earlier

Incidence of anaemia-defined as low haemoglobin and/or haematocrit requiring blood transfusion or DIC - disseminated coagulopathy or ductus arteriosus treatment or hypotensive treatment

Neonatal sepsis

Time Frame: anytime after the recruitment visit or after delivery before discharge from the hospital or up to 6 weeks after delivery if discharged earlier

Incidence of confirmed bacteraemia in cultures or necrotizing enterocolitis - Necrotising enterocolitis (NEC)

Secondary Outcomes

  • Maternal anxiety levels(at the recruitment visit and every 2 weeks until delivery)
  • Onset of labour(through study completion, an average of 5 weeks after the recruitment visit)
  • Number of hospital visits(after the recruitment visit until delivery)
  • Compliance(after the recruitment visit until delivery)
  • Preeclampsia(between 20 weeks' gestation - up to 6 weeks after birth)
  • Mode of delivery(through study completion, an average of 5 weeks after the recruitment visit)
  • Gestational hypertension(between 20 weeks' gestation - up to 6 weeks after birth)

Study Sites (1)

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