Actively Recruiting
The Role of Ultrasonography in Labor in Predicting the Outcomes of Childbirth
Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2025-02-04
116
Participants Needed
1
Research Sites
382 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Ultrasound in the delivery room represents a useful diagnostic tool and is used for the assessment of fetal presentation, fetal malpresentation/malposition, and prior to any operative delivery. Transperineal ultrasonography, performed by placing the ultrasound probe covered by a sterile glove at the level of the labia majora, has proven useful in providing information on the progression of the presented fetal part in the birth canal and in predicting birth outcomes. Many studies have shown a correlation between the above ultrasound indices and birth outcomes. These ultrasound indices are therefore used in clinical practice to assess the progression of the presented fetal part in the birth canal and the presence of fetal malpresentation/malposition. Despite this, to date, few studies have evaluated the correlation between dynamic changes in these ultrasound parameters between rest and maximal maternal pushing during the second stage of labor and birth outcomes. Knowing before delivery which parameters are suggestive of possible dystocia would allow the clinician to adopt therapeutic strategies aimed at resolving them and thus increase the rate of spontaneous vaginal deliveries. The investigators want to evaluate the role of an ultrasound parameter obtained by transabdominal ultrasound in the second stage of labor, the occiput-column angle, in predicting spontaneous delivery vaginally in fetuses with transverse occiput
CONDITIONS
Official Title
The Role of Ultrasonography in Labor in Predicting the Outcomes of Childbirth
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women aged 60 18 years
- Single pregnancy at term (37-42 gestational weeks)
- Fetus in cephalic presentation and in expulsive period (complete cervical dilatation and premature sensation)
- Acquisition of informed consent form
You will not qualify if you...
- Placenta previa
- Uterine malformations
- Previous uterine surgery
- Cardiotocographic tracing (CTG) abnormalities
- Any contraindication to vaginal delivery
AI-Screening
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Trial Site Locations
Total: 1 location
1
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Bologna, Bologna, Italy, 40138
Actively Recruiting
Research Team
A
Aly Mohamed Alaaeldin Kamaleldin Aly Youssef, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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