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Inhaled Salbutamol in Elective Caesarean Section

Phase 4
Conditions
Cesarean Section
Postnatal Pulmonary Adaptation
Interventions
Drug: Placebo
Registration Number
NCT01978418
Lead Sponsor
Sture Andersson
Brief Summary

The lungs of the fetus are filled with fluid and it is essential that fetal lung fluid is cleared at birth. This process is mediated through the activation of airway epithelial sodium channels (ENaC). In animals, ENaC is considered crucial for postnatal pulmonary adaptation. In humans, postnatal ENaC expression is dependent on gestational age and its activity, measured as nasal potential difference, correlates with lung compliance. Therefore, in the human newborn infant ENaC may be important for physiologic postnatal adaptation. The activity of ENaC is increased by beta-agonists, such as salbutamol. We hypothesize that low pulmonary expression or activity of ENaC in the perinatal period causes delayed clearance of lung fluid and thereby contributes to the risk for development of transient tachypnea of the newborn (TTN) in term infants born by Caesarean section (CS).

Detailed Description

We hypothesize that low pulmonary expression or activity of ENaC in the perinatal period causes delayed clearance of lung fluid and thereby contributes to the risk for development of transient tachypnea of the newborn (TTN) in term infants born by Caesarean section (CS). The aim of this study is to evaluate whether the respiratory status, measured by a transthoracic ultrasound method and lung compliance, of newborns infants born by CS can be improved by inhaled salbutamol at 30-60 minutes of age. 62 infants will be included and randomized to receive salbutamol or placebo-inhalations in a double-blind manner.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
62
Inclusion Criteria
  • healthy singleton pregnancy
  • Cesarean section at 37 + 0 to 41 + 6 gestational weeks
Exclusion Criteria
  • clinically significant congenital malformations
  • birth weight < 2000 grams
  • intubation
  • 200 bp for more than 5 min
  • relevant medication of the mother, e.g. albetol, beta-agonists (e.g. salbutamol, salmeterol), corticosteroids
  • the suspicion of/confirmed pneumothorax or infection

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PlaceboPlaceboPlacebo is administered once, at 30-60 minutes of age
InterventionsalbutamolSalbutamol 0,4 mg inhalation, given once at 30-60 minutes of age
Primary Outcome Measures
NameTimeMethod
To evaluate whether lung ultrasound at 30-60 minutes of birth is improved at 3-6 hours of birth6 hours

To evaluate whether the respiratory status measured by a transthoracic ultrasound method of newborn infants born by CS can be improved by inhaled salbutamol at 30-60 minutes of age.

Secondary Outcome Measures
NameTimeMethod
To evaluate whether lung compliance measured at 3-6 hours is improved by inhaled salbutamol at 30-60 minutes of age6 hours

To evaluate whether lung compliance of newborn infants born by CS can be improved by inhaled salbutamol at 30-60 minutes of age.

Decrease in respiratory rate at 3-6 hours of age6 hours

To see whether respiratory rate is decreased in infants receiving salbutamol at 30-60 minutes of age

To see whether there is a correlation between airway ENaC expression measured at 30-60 minutes of age and consequent lung fluid content at 3-6 hours of age6 hours
Whether cord blood cortisol concentrations correlate with expression of ENaC and further, with decrease in lung fluid content at 3-6 hours of age6 hours of age

whether cord blood cortisol concentrations correlate with expression of ENaC and further, with decrease in lung fluid content at 3-6 hours of age

Trial Locations

Locations (1)

Women's Hospital

🇫🇮

Helsinki, Finland

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