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Fetal Weight clinical trials

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NCT ID: NCT06232187 Enrolling by invitation - Ultrasound Clinical Trials

AI Support in Novice's Decision-making for Ultrasound Fetal Weight Estimation

scan-AId
Start date: February 14, 2024
Phase: N/A
Study type: Interventional

The SCAN-AID study is a prospective, randomized, controlled, and unblinded study that compares the performance of novices in ultrasound fetal weight estimation. The study evaluates the impact of two levels of AI support: a straightforward black box AI and a more detailed explainable AI.

NCT ID: NCT05530616 Completed - Fetal Weight Clinical Trials

Impact of Ultrasound Fetal Weight Estimation on Obstetrical Management and Maternal and Neonatal Outcomes

EPF
Start date: May 13, 2022
Phase:
Study type: Observational

The investigators wish to study the obstetrical data of pregnant women who had an ultrasound estimation of fetal weight and who delivered at the University Hospital of Strasbourg over the last 20 years. These retrospectively collected data are a valuable source of scientific information since they are "real life data", currently of growing interest in the scientific community, and have a large volume and quality due to the number of years included and the variety of information collected in the computerized media records. From this study, the investigators hope not only to better understand the consequences of ultrasound screening for fetal growth, but also to improve its accuracy and to develop useful models in obstetrical decision making in order to decrease maternal and neonatal morbidity.

NCT ID: NCT05478798 Not yet recruiting - Pregnancy Related Clinical Trials

Comparison of Three Methods for Fetal Weight Estimation

Start date: August 1, 2022
Phase:
Study type: Observational

The aim of this study was to compare maternal, clinical and ultrasound estimations of fetal weight in women with severe (BMI>35) and morbid (BMI>40) obesity and to determine the effect of maternal body mass index (BMI) on these estimations.

NCT ID: NCT05362175 Completed - Birth Weight Clinical Trials

Cross Sectional Area of Umbilical Cord Versus Hadlock's Formula in Prediction of Neonatal Birth Weight

Start date: July 15, 2021
Phase:
Study type: Observational

Ultrasound measurement of cross sectional area of umbilical cord might offer advantage over Hadlock's formula for accurate estimation of actual birth weight at term gestation leading to prevention of large number of maternal and neonatal morbidity and mortality.

NCT ID: NCT05197101 Not yet recruiting - Macrosomia, Fetal Clinical Trials

To Evaluate the Efficacy and Safety of Balloon Catheter Combined With Oxytocin Induction in Nulliparous Women With Estimated Fetal Weight ≥3500g at 39-40 Weeks of Gestation

Start date: January 17, 2022
Phase: N/A
Study type: Interventional

This study is a randomized, controlled, observational study. 150 nulliparous women with estimated fetal weight ≥3500g at 39-40 weeks of gestation will be enrolled as subjects in the two groups is 1:1. In the experimental group, vaginal examination will be performed at 39 to 40 weeks to assess cervical conditions. If the bishop score <6, the balloon catheter combined with oxytocin induction will be planned at 40 weeks ±3 days. In the control group, one week to 41 weeks ±3 days will be expected. Vaginal examination will be performed again to evaluate cervical conditions. If the bishop score <6 points, and balloon catheter combined with oxytocin induction will be performed. After 96h, their final delivery mode will be recorded. In the following 42 days postpartum, their complications and the neonatal outcome will be followed up.

NCT ID: NCT03962153 Completed - Clinical trials for Fetal Growth Abnormality

Ultrasonographic Parameters for Fetal Weight Prediction

Start date: January 1, 2019
Phase:
Study type: Observational

The hypothesis is to increase the predictability of the ultrasound examination evaluating new fetal parameters: in fact the thickness of the soft tissues can contribute significantly to the fetal weight and the characteristics of the thoracic cage may correlate with the fetal weight.

NCT ID: NCT03857204 Not yet recruiting - Fetal Weight Clinical Trials

Fetus Weight Estimation by Ultrasound Data Collection

Start date: March 1, 2020
Phase: N/A
Study type: Interventional

This research aims to allow deployment & optimization of SAMPL plain wave algorithm so as to make required advancement towards a light-weight portable US platform or wireless probe - thus elevating clinician's care level and patient treatment by allowing more scan availability and flexibility.

NCT ID: NCT03459989 Recruiting - Clinical trials for Estimation of Fetal Weight

Comparison Between Fetal Thigh Soft Tissue Versus Hadlock's Formula in Estimation of Fetal Weight by Ultrasound

STT
Start date: May 15, 2017
Phase:
Study type: Observational

We are going to do 2d ultrasound to compare between hadlock's formula and thigh soft tissue formula in expecting the after birth fetal weight and to find which of these formulas to be more accurate

NCT ID: NCT03321435 Completed - Placenta Previa Clinical Trials

The Placenta Previa and Fetal Weight

Start date: October 1, 2016
Phase: N/A
Study type: Observational

Placenta previa is a placenta that implants at lower uterine segment, it occurs in about 0.3-0.5% of pregnancies at term. It is a significant risk for development of maternal morbidity, as well as maternal mortality secondary to maternal hemorrhage . Also, this abnormal placenta has a negative concern about fetal well being due to prematurity and perinatal mortality, in addition to its undesirable effect on fetal growth. Several factors may be behind of the effect of placenta previa on fetal growth. Firstly, the blood supply to the lower uterine segment is less than at the upper segment apparently resulting in less feto-placental blood perfusion . Secondly, recurrent bleeding attacks from placental previa may affect fetal oxygenation and fetal growth. In spite of above evidences; many studies in literature denied the relation between placenta previa and fetal growth and concluded that the association between low birth weight and placenta previa is mainly due to preterm delivery and to a lesser extent with fetal growth restriction. However; the major drawback of all these studies is lacking of reporting the effect of placenta previa of feto-maternal blood flow representing in studying of Doppler blood flow in both uterine and umbilical artery in those patients. The uterine artery blood flow is usually affected by the presence of placenta previa and placenta accreta which reflected on feto-placental blood flow. So the uterine artery Doppler velocimetry is a useful tool for predicting placenta accreta . So in the light of above evidences; we aimed, in the current study, not only to investigate the effect on placenta previa on fetal weight but also to walk around the effect of placenta previa on the uterine and umbilical arteries blood flow in trial to explore this conflicting issue. To our knowledge, no previous trial had studied this interesting subject before.

NCT ID: NCT03206281 Not yet recruiting - Clinical trials for Ultrasonography, Prenatal

Tall Stature Women Fetal Weight Estimation

TSFW
Start date: July 5, 2017
Phase: N/A
Study type: Observational [Patient Registry]

To investigate the difference of clinical VS sonographic fetal weight estimation of tall women stature (above 10t percentile)