- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06806904
The Role of Ultrasonography in Labor in Predicting the Outcomes of Childbirth (EcoSP_21)
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
Study Overview
Status
Conditions
Detailed Description
Participants will be recruited at the time of admission or in the delivery room. Routine clinical practice involves transabdominal ultrasound, performed in the lithotomy position, placing the probe transversely and longitudinally at the abdominal level for evaluation of the fetal situation and presentation.
In addition to normal ultrasound, the position of the fetal occiput will also be assessed in women who agree to participate in the study, and in fetuses with a transverse occiput, the occipitecolumn angle will be measured. All study participants will then undergo transperineal ultrasound, performed by placing the probe, covered by a sterile glove, at the level of the labia majora, first longitudinally and then transversely. In this way, a series of ultrasound landmarks will be visualized: pubic symphysis, bladder, urethra, vagina, rectum, pubo-rectal muscle, and fetal head.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Aly Mohamed Alaaeldin Kamaleldin Aly Youssef, MD
- Phone Number: 0512144412
- Email: aly.youssef@aosp.bo.it
Study Locations
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Bologna, Italy, 40138
- Recruiting
- IRCCS Azienda Ospedaliero-Universitaria di Bologna
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Contact:
- Aly Mohamed Alaaeldin Kamaleldin Aly Youssef, MD
- Phone Number: 0512144412
- Email: aly.youssef@aosp.bo.it
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Women aged >= 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
Exclusion Criteria:
- Placenta previa
- Uterine malformations
- Previous uterine surgery
- Cardiotocographic tracing (CTG) abnormalities
- Any contraindication to vaginal delivery
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Measurement of Angle of Progression (AoP)
Time Frame: At the time of delivery: at rest and during maternal pushing
|
Angle of progression (AoP): the angle between the longitudinal axis of the pubic symphysis and a straight line starting from the lower edge of the symphysis and passing tangentially to the most distal part of the fetal head
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At the time of delivery: at rest and during maternal pushing
|
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Measurement of Anteroposterior Pelvic Hiatus Diameter (APD)
Time Frame: At the time of delivery: at rest and during maternal pushing
|
Anteroposterior pelvic hiatus diameter (APD): distance between the posteroinferior margin of the pubic symphysis and the anterior margin of the pubo-rectal muscle
|
At the time of delivery: at rest and during maternal pushing
|
|
Measurement of Head-Sympanic Distance (HSD)
Time Frame: At the time of delivery: at rest and during maternal pushing
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Head-symphysis distance (HSD): distance between the lower edge of the pubic symphysis and the nearest point of the fetal scalp along the infrapubic line
|
At the time of delivery: at rest and during maternal pushing
|
|
Measurement of Head-Perineum Distance (HPD)
Time Frame: At the time of delivery: at rest and during maternal pushing
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Head-Perineum Distance (HPD): distance between the perineum and the nearest point of the fetal scalp
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At the time of delivery: at rest and during maternal pushing
|
Collaborators and Investigators
Investigators
- Principal Investigator: Aly Mohamed Alaaeldin Kamaleldin Aly Youssef, MD, IRCCS Azienda Ospedaliero-Universitaria di Bologna
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- EcoSP_21
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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