Oxidative Stress in Women Treated With Atosiban for Impending Preterm Birth
- Registration Number
- NCT03570294
- Lead Sponsor
- Polish Mother Memorial Hospital Research Institute
- Brief Summary
Oxidative stress is recognized as a important factor in the pathogenesis premature birth. Preterm birth is defined as delivery before 37 completed weeks of gestation and it is the leading cause of neonatal morbidity and mortality. The investigators conducted this analysis to investigate the safety of administration of Atosiban - a reversible, competitive antagonist of the oxytocin receptor in the treatment of preterm labor and its impact on the level of oxidative stress after 48 hours of tocolytic treatment.
- Detailed Description
Atosiban (1-(3-mercaptopropanoic acid)-2-(O-ethyl-D-tyrosine)-4-L-threonine-8-L-ornithine-oxytocin) is licensed for clinical use in women suffering from threatened premature birth and is widely used in clinical practice in Europe because of its low side effect profile. The impact of Atosiban on pregnancy outcomes in women has been investigated in recent years and the research has shown its ability to reduce intracytoplasmic calcium release and downregulate prostaglandin synthesis as oxytocin receptor antagonist. While a role of Atosiban in the modulation of myometrial contractility is well-described, its effect on many other functions is not so well known.
The serum and plasma samples take for the measurement of total oxidant status (TOS), total antioxidant status (TAS), level of 3-nitrotyrosine (3-NT), and carbonyl and thiol groups will be stored at -70°C in aliquots for subsequent biochemical analysis and processed within two months.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 64
- pregnant women between 24-35 weeks' gestation receiving prenatal care due to the risk of premature birth
- intact membranes
- evidence of premature labor (regular, painful and persistent uterine contractions; cervical changes)
- acute fetal distress
- other conditions requiring immediate delivery (eclampsia and severe pre-eclampsia, placenta previa, abruptio placenta)
- vaginal bleeding,
- premature rupture of membranes
- chorioamnionitis,
- fetal congenital malformations,
- intrauterine growth restriction,
- the use of any tocolytic drugs during pregnancy before admission to the hospital
- circulatory system diseases (e.g. heart defects, hypertension),
- symptoms of infection
- other diseases that may increase oxidative stress
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Atosiban Atosiban Total oxidant status (TOS), total antioxidant status (TAS) and oxidative stress index (OSI) values as well as 3-nitrotyrosine, carbonyl and thiol groups levels weill be measure using ELISA test in serum and plasma of 64 pregnant women before and after 48 hours of continuous administration of Atosiban.
- Primary Outcome Measures
Name Time Method Delay preterm delivery for 48 hours 48 hours Delay preterm delivery for 48 hours, thus allowing administration of corticosteroids to induce surfactant production in fetal lungs and improve neonatal outcome
- Secondary Outcome Measures
Name Time Method Apgar score At birth Apgar score
Weight At birth Weight
Time to delivery measured from start of Atosiban administration Up to 15 weeks from start of Atosiban administration Time to delivery measured from start of Atosiban administration
Incidence of duration of hospitalization Up to 28 days after birth Incidence of duration of hospitalization
Trial Locations
- Locations (1)
Department of Obstetrics, Perinatology and Gynecology, Polish Mother's Memorial Hospital-Research Institute
🇵🇱Łódź, Poland