This is a prospective, randomized trial to determine whether the use of sonographic parameters during labor results in less intrapartum infection compared to traditional invasive examination. Other secondary outcomes include maternal satisfaction and overall birth outcomes.
Age range
18 Years – 60 Years
Sex
FEMALE
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Maternal Fever Incidence
Timeframe: In the course of labour from admission until delivery in 3-4 hour intervals
Maternal Tachycardia Incidence
Timeframe: In the course of labour from admission until delivery in 3-4 hour intervals
Maternal Leucocytosis
Timeframe: In the course of labour from admission until delivery in 6 hour intervals
Uterine tenderness
Timeframe: In the course of labour from admission until delivery 3-4 hour intervals
Fetal Tachycardia
Timeframe: In the course of labour from admission until delivery
Foul-smelling amniotic fluid
Timeframe: In the course of labour from admission until delivery