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Breech Presentation clinical trials

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NCT ID: NCT06339164 Not yet recruiting - Clinical trials for Breech Presentation; Before Labor

Breech Delivery Skills. Resident Learning Program

Breech
Start date: April 15, 2024
Phase:
Study type: Observational

Breech delivery is one of the mail topic in emergency obstetrics for Italian Board of Obstetrics and Gynecology. Formal frontal lecture and digital learning represent nowadays the two typical learning methods. A bedside evaluation it's not feasible due to rarity of such emergency, due to the common senior physicians involvement when it occurs, and due to medico-legal risks. Mannequin scenario represents the best way of skill evaluation

NCT ID: NCT06187948 Recruiting - Breech Presentation Clinical Trials

An Informative Video Before Planned External Cephalic Version

Start date: December 26, 2023
Phase: N/A
Study type: Interventional

A randomized control trial to investigate whether an informative video before planned external cephalic version reduces maternal anxiety and improves chances of success.

NCT ID: NCT05827627 Completed - Breech Presentation Clinical Trials

Simulation Techniques Used in Breech Birth Management Training

Start date: November 10, 2019
Phase: N/A
Study type: Interventional

This study was conducted to assess the effect of two different simulation techniques that are used to improve breech birth management skills of midwifery students on the anxiety, self-efficacy, skill and knowledge levels of students.

NCT ID: NCT05224908 Recruiting - Pregnancy Related Clinical Trials

Breech Pelvimetry by EOS® Technique With Change of Maternal Position and Delivery Route

PelviEOS
Start date: January 26, 2022
Phase: N/A
Study type: Interventional

When a patient presents with a fetus in PS after 36+0SA, after acceptance of participation in the study, pelvimetry with evaluation of the height of the fetal presentation by EOS® system in the upright and sitting position will be performed. CT pelvimetry will not be performed. The patient may then be offered an attempt at VME, with clear, fair and appropriate information, after being informed of the data from the right standing EOS® pelvimetry (report and images). VME will be performed according to the recommendations and practice of the department. In the event of failure with a fetus that remains in PS, the choice of delivery route will be decided in consultation with the patient after clear, fair and appropriate information. If the patient wishes to have a vaginal delivery, the pregnancy will be continued without intervention until spontaneous labour or induction in case of indication (premature rupture of membranes (PMR), over term, or intercurrent maternal or fetal pathology). The modalities of the delivery route and/or a possible induction will be discussed between the obstetric team and the patient. If the patient wishes a caesarean delivery in case of persistent PS, the delivery will be scheduled after 39+0SA or earlier if indicated (RPM, intercurrent maternal or fetal pathology). In the case of a successful VME with a fetus that remains in cephalic presentation until labour, management will follow current recommendations. The characteristics of the dimensions and angles of the obstetric pelvis and the height of the fetal presentation in the standing and sitting positions, the performance and success of MEC, the choice of delivery route, and the final delivery route will be recorded.

NCT ID: NCT04849975 Completed - Clinical trials for Breech Fetal Presentation

Comparison of Pelvimetric Measurements Between MRI and Low-dose Stereoradiography (EOS® Imaging System)

CAPEOS®
Start date: November 9, 2021
Phase: N/A
Study type: Interventional

The main objective of this study is to compare pelvimetric measurements performed by Magnetic Resonance Imaging (MRI) and by the EOS imaging system.

NCT ID: NCT04613778 Recruiting - Breech Presentation Clinical Trials

Correction of Breech Presentation With Laser Acupuncture

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

Acupuncture-type interventions (such as moxibustion and acupuncture) at Bladder 67 (BL67, Zhiyin point) have been proposed to have positive effects on breech presentation. However, the role of laser acupuncture for Breech presentation remains unknown. The aim of this study is to evaluate the effectiveness and safety of laser acupuncture in correcting breech presentation.

NCT ID: NCT04585256 Recruiting - Clinical trials for Breech Presentation of Fetus With Successful Version

Trendelenburg Positioning and External Cephalic Version Outcome

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

Women at term (over 37 weeks) that are candidates for external cephalic version will be positioned in the trendelenburg position 5 minutes prior to external cephalic version performance and during the procedure. The control group will not be positioned differently than usual. We will evaluate external cephalic version success and compare the 2 groups.

NCT ID: NCT04579835 Recruiting - Breech Presentation Clinical Trials

Twin A Breech External Cephalic Version Intervention Trial (TWEXIT)

TWEXIT
Start date: September 28, 2020
Phase:
Study type: Observational

A prospective study assessing the use of external cephalic version for the management of Twin A breech presentation in twin pregnancy.

NCT ID: NCT04538261 Terminated - Breech Presentation Clinical Trials

Elevation of the Fetal Buttocks Prior to External Cephalic Version

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

This is a prospective, randomized double-blind clinical trial evaluating the effect of a balloon device (Fetal Pillow) to elevate the fetal buttocks during external cephalic version procedures. Eligible study population: nulliparous pregnant women between 37-40 weeks estimated gestational age with a breech presenting fetus and no contraindications to external cephalic version.

NCT ID: NCT04118465 Completed - Clinical trials for Breech Presentation; Before Labor

Prospective Randomized Controlled Trial Comparing ECV Success Rates With and Without Full Urinary Bladder

ECVBLADDER
Start date: January 2002
Phase: N/A
Study type: Interventional

A comparison of external cephalic (ECV) success rates when ECV performed with full urinary bladder or not. The study is prospective and randomised. Both nulliparous and multiparous women will be enrolled in the study, however each group will be randomized separately either to full urinary bladder or not. Written informed consent will be obtained prior to inclusion in the study.