Rationale: Severe, early-onset fetal growth restriction (FGR) due to placental insufficiency is associated with a high risk of perinatal morbidity with long-lasting sequelae and mortality. Placental insufficiency is the result of abnormal formation and function of the placenta (placentation) with inadequate remodelling of the maternal spiral (uteroplacental) arteries. There is currently no therapy available with demonstrated effectiveness. Evidence suggests Sildenafil citrate improves uteroplacental blood flow, growth, and meaningful outcomes. Objective: To evaluate the effectiveness of sildenafil (versus placebo) in achieving healthy perinatal survival. Study design: Multicenter nationwide randomized placebo-controlled clinical trial. Study population: Women with a singleton pregnancy between 20 and 30 weeks with severe fetal growth restriction of likely placental origin, and with estimated significant likelihood of perinatal death. Intervention: Sildenafil 25mg or placebo tablet orally three times daily. Main study parameters/endpoints: Perinatal healthy survival, i.e. survival without severe neonatal morbidity at term age. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Taking tablets three times daily. No additional ultrasounds, other than standard clinical protocol, one extra blood sample at inclusion. No risks anticipated, unexpected medication-associated risks can't be excluded on beforehand.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
216
Sildenafil 25 mg three times daily orally from randomization until delivery
Placebo tablets three times daily orally from randomization until delivery
Radboud Medisch Centrum Nijmegen
Nijmegen, Gelderland, Netherlands
Maastricht Universitair Medisch Centrum
Maastricht, Limburg, Netherlands
Maxima Medisch Centrum
Veldhoven, North Brabant, Netherlands
Vrije Universiteit Medisch Centrum
Amsterdam, North Holland, Netherlands
Academisch Medisch Centrum
Amsterdam, North Holland, Netherlands
Isala Klinieken
Zwolle, Overijssel, Netherlands
Leids Universitair Medisch Centrum
Leiden, South Holland, Netherlands
Erasmus Medisch Centrum Rotterdam
Rotterdam, South Holland, Netherlands
Universitair Medisch Centrum Groningen
Groningen, Netherlands
Universitair Medisch Centrum Utrecht
Utrecht, Netherlands
Intact neonatal survival until term age
Time frame: Term age, up to 20 weeks after randomization
Fetal growth velocity assessed by ultrasound: abdominal circumference measurements (AC)
Average daily increase in ultrasound-estimated AC
Time frame: At contact moments with the patient, up to 20 weeks after randomization
Age-adequate performance on the two-year Bayley scales of infant development (BSID)-III (composite cognitive score and composite motor score)
Time frame: 2 years corrected age, up to 2 years and three months after randomization
Co-incidence and severity of the maternal syndrome of pre-eclampsia / HELLP-syndrome (Hemolysis Elevated Liver enzymes Low Platelets)
Time frame: At contact moments with the patient, up to 20 weeks after randomization
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