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Dystocia clinical trials

View clinical trials related to Dystocia.

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NCT ID: NCT06442735 Completed - Clinical trials for Complication of Delivery

Clinical Application of Intrapartum Ultrasound

IPUS
Start date: January 1, 2022
Phase: N/A
Study type: Interventional

Intrapartum ultrasound monitoring is to be compared with conventional labor monitoring to clarify the accuracy of this technology, and then provide a basis for later related research.

NCT ID: NCT06438081 Not yet recruiting - Delivery Problem Clinical Trials

Comparison Between Propess and Cook Double-balloon Catheter for Cervical Priming: a Randomized Controlled Trial

Start date: June 1, 2024
Phase: Phase 4
Study type: Interventional

We aimed to compare efficacy and safety of Propess versus Cooks double-balloon catheter for cervical ripening with an unfavorable cervix in term pregnancy.

NCT ID: NCT06283277 Not yet recruiting - Macrosomia, Fetal Clinical Trials

Fetal Clavicular Measurement to Predict Fetal Macrosomia

Start date: May 1, 2024
Phase:
Study type: Observational

Macrosomia is associated with increased risks for both the mother and the baby, including complications during delivery, injuries, and even death. The accurate diagnosis of macrosomia is often difficult before birth. There are a number of factors that can increase the risk of macrosomia, such as maternal obesity, diabetes, and excessive weight gain during pregnancy. There are also a number of different techniques that can be used to try to predict macrosomia, but none of them are perfect. The aim of this study is to evaluate sensitivity of measuring fetal clavicle length in third trimester compared with biacromial diameter and Hadlock formula IV for prediction of fetal macrosomia.

NCT ID: NCT06268431 Recruiting - Prolonged Labor Clinical Trials

Oxytocin Rest to Reduce Cesarean Delivery

ORCA
Start date: February 15, 2024
Phase: N/A
Study type: Interventional

Prolonged labor is usually managed with continuous oxytocin infusion. "Oxytocin rest" has been proposed as a strategy to resolve protracted labor in patients who have received continuous oxytocin without progress. This strategy involves discontinuing oxytocin then restarting infusion after a period of time, under the theory that washout of the oxytocin receptor will strengthen uterine contractions to improve labor progress. "Oxytocin rest" is performed on labor and delivery units across the United States. Yet, there is no randomized or prospective data to support the practice. The purpose of this study is to assess whether oxytocin rest of 60 minutes in patients with prolonged labor reduces risk for cesarean delivery.

NCT ID: NCT06249061 Not yet recruiting - Labour Dystocia Clinical Trials

Oral Sodium Bicarbonate for the Prevention of Labour Dystocia

Labour-Aide
Start date: June 2024
Phase: N/A
Study type: Interventional

Sodium bicarbonate is often used by athletes to improve their muscle's ability to contract and power their activity. It works by decreasing the risk of lactic acid build-up, which causes cramping and fatigue. Some research suggests that using sodium bicarbonate in labour could help to improve the ability of the uterus to contract, helping to prevent labour dystocia (stalled or slow progress in labour). This could ultimately increase the chance of spontaneous vaginal delivery. This research is being done to investigate whether drinking sodium bicarbonate (commonly known as baking soda) dissolved in water as a hydration drink could benefit women in labour and increase the chance of a vaginal birth. In order to answer this question, pregnant people from London, Markham and Mississauga midwifery practices are being recruited to participate in this study. Participants will be randomly assigned to one of two groups when they are admitted to hospital in labour. One group will be asked to drink normal fluids of their choice while they are in labour (usual care). The second group will be asked to consume a drink made of baking soda and water, as well as normal fluids of their choice. Mode of birth and the use of birth interventions will be compared between the two groups. Infant outcomes will be compared to ensure that the use this drink in labour is safe. A risk of consuming sodium bicarbonate is gastrointestinal disturbance. The number of people who reported gastrointestinal upset will also be compared between the two groups. If this study shows that those who drank sodium bicarbonate in labour had an increased chance of vaginal birth and that it is safe, this low-cost, low-risk treatment has the potential to reduce birth interventions for pregnant people and their babies.

NCT ID: NCT06105268 Recruiting - Clinical trials for Shoulder Dystocia - Delivered

Management of Shoulder Dystocia in Flipped Learning

Start date: June 6, 2023
Phase: N/A
Study type: Interventional

Flipped learning is an innovative learning method in midwifery education. Studies that apply this learning method together with shoulder dystocia training have not been found in the current literature. For this reason, the study was designed as a randomized controlled study to examine the effectiveness of the flipped learning technique in shoulder dystocia management using high-valid simulation in midwifery undergraduate education.

NCT ID: NCT05962918 Completed - Clinical trials for Satisfaction, Patient

Perineal Massage Performed During the Labour

Start date: December 1, 2018
Phase: N/A
Study type: Interventional

In this study, perineal massage was applied to primiparous women who did not give birth before, as a quasi-experimental control group to determine the effects of massage on birth comfort, perineal trauma and perineal pain.

NCT ID: NCT05921045 Completed - Birth Disorder Clinical Trials

Learning Skills in Shoulder Dystocia Delivery Using Simulator Models

Start date: January 1, 2023
Phase:
Study type: Observational [Patient Registry]

Learning skills on shoulder dystocia on doctor and midwife

NCT ID: NCT05913609 Recruiting - Shoulder Dystocia Clinical Trials

Safety and Effectiveness of the Yaari Extractor for Management of Shoulder Dystocia

Start date: November 15, 2023
Phase: N/A
Study type: Interventional

Prospective, multi-center, single arm with historical control, to verify the safety and effectiveness of the Yaari Extractor used by board certified or board eligible U.S. OB/GYN physicians in the management of shoulder dystocia.

NCT ID: NCT05881629 Not yet recruiting - Labor Complication Clinical Trials

Early Diagnosis and Intervention for Fetal Malposition in Active Labor and Its Impact on Mode of Delivery

Start date: April 28, 2024
Phase: N/A
Study type: Interventional

The goal of this randomized trial is to test if changing a person's position in labor can increase the chances of delivering their baby vaginally. Specifically, it aims to answer the questions: - In fetuses who are facing upwards (occiput posterior, OP) or sideways (occiput transverse, OT) during labor, does changing the patient's position during active labor to a side-lying posture with a peanut ball increase the chances of them having a successful, spontaneous vaginal delivery? - Does changing the patient's position in active labor affect the position of the baby at the time of delivery? - Do intentional position changes in labor impact patient-perceived autonomy during their labor and delivery experience? Participants will: - Receive an ultrasound during labor to determine the position of their baby - Be asked to adopt a specific position in labor (side-lying with peanut ball) if they are randomized to the study group - Receive additional ultrasounds during labor to assess their baby's position - Fill out a questionnaire about their labor experience following the delivery of their baby