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Breech Presentation clinical trials

View clinical trials related to Breech Presentation.

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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: 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: 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: NCT03827226 Recruiting - Breech Presentation Clinical Trials

Breech External Cephalic Version Intervention Trial

BREXIT
Start date: February 5, 2019
Phase:
Study type: Observational

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

NCT ID: NCT02801201 Recruiting - Breech Presentation Clinical Trials

Impact of Analgesia on Success of External Version: Comparison of Spinal Anesthesia Versus Sedation

RaVem
Start date: May 31, 2016
Phase: Phase 3
Study type: Interventional

At the time of birth, nearly 5% of children are in breech presentation. This type of presentation requires a medical environment and leads to more frequent use of Caesarean sections. This is why the external version can be proposed, usually from the 36th week. Its success rate is 40%, and is usually performed under simple sedation. One of the causes of failure is the lack of relaxation of the uterus, which could be higher in case of deeper anesthesia, as is the case in spinal anesthesia. The study project is to demonstrate superiority of spinal anesthesia compared to the usual protocol sedation in terms of primary and secondary objectives.

NCT ID: NCT01564004 Recruiting - Clinical trials for Breech Presentation at Term

Clinical Hypnosis Before External Cephalic Version (ECV)

Start date: February 2011
Phase: N/A
Study type: Interventional

Does clinical hypnosis or neuro-linguistic programming improve the success rate of external cephalic version?