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Dystocia clinical trials

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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: 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: NCT05660551 Completed - Shoulder Dystocia Clinical Trials

Investigation of the Effect of Different Training Techniques in Teaching the Management of Shoulder Dystocia

Start date: December 23, 2022
Phase: N/A
Study type: Interventional

In this study, it was aimed to determine the effect of demonstration, telesimulation and game-based teaching on teaching shoulder dystocia management in midwifery students. H01: There is no difference between the four groups in terms of satisfaction with learning. H02: There is no difference between the four groups in terms of Self-Confidence in Learning. H03: There is no difference between the four groups in terms of Motivation scores in Teaching Materials.

NCT ID: NCT05582135 Completed - Analgesia Clinical Trials

Postoperative Analgesic Effect of Esketamine

Start date: May 5, 2021
Phase: N/A
Study type: Interventional

The aim of this study was to determine whether the addition of esketamine to morphine would improve postoperative analgesia after caesarean section. Parturients who planned for a caesarean delivery using combined spinal-epidural anaesthesia with a request for postoperative anaesthesia were randomly divided into four groups (A, B, C and D). When the surgery was completed, the parturients in groups A, B, C and D were administered 2 mg morphine, 0.25mg/kg of esketamine, 0.25mg/kg of esketamine plus 2 mg morphine sulfate and 0.25mg/kg of esketamine plus 1 mg morphine through the epidural catheters, respectively. The postoperative pain at rest, pain with movement, the number of rescue analgesics and adverse effects were evaluated for 48 h after caesarean delivery.

NCT ID: NCT05155826 Completed - Labor Pain Clinical Trials

Effect of Virtual Reality for Pain Management During Intracervical Balloon Placement for Artificial Childbirth Induction

VIRTUALMAG
Start date: February 1, 2022
Phase: N/A
Study type: Interventional

The labor induction concerns 22% of births in France. In the event of labor induction, in almost two thirds of cases, a cervical ripening method is used and the use of mechanical methods is observed for 8% of cervical ripening. Intra-cervical balloon placement is generally well tolerated but is frequently associated with pain and acute anxiety. There are few options for pain relief. Virtual reality, a relatively new intervention, has been studied as a distraction technique for pain relief, but never in the context of the induction of childbirth.

NCT ID: NCT04741698 Completed - Labor Dystocia Clinical Trials

Propranolol for Protracted Labor

PRO-Labor
Start date: July 27, 2021
Phase: Phase 1
Study type: Interventional

Induction of labor is one of the most common procedures performed on labor and delivery. In the United States, more than 20 percent of pregnant women undergo an induction of labor [1]. There is data from small, randomized studies that demonstrates the effectiveness of propranolol, a non-selective beta-blocker, for labor augmentation. This literature suggests a decrease in the amount of time to delivery and a possible reduction in cesarean section rates when propranolol is used in conjunction with oxytocin for induction of labor compared to oxytocin alone [2-8]. Alpha- and beta-adrenergic receptors have been identified in the human myometrium. Propranolol has been shown in studies to enhance uterine contractions and may be a useful tool in this population of women. Therefore, the purpose of this study is to assess whether the administration of propranolol at time of labor dystocia reduces time to delivery.

NCT ID: NCT04649593 Completed - Dystocia Clinical Trials

The Study of Giving Birth, a Study About Treatment of Labor Dystocia

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

Labor dystocia is an intransigent, high-profile issue in obstetric care, which causes significant maternal morbidity in low resource settings and maternal dissatisfaction, and increased healthcare costs worldwide. Amniotic fluid lactate, (AFL), values have recently been shown to reflect the metabolic status of the uterus and high levels have a strong association with subsequent need for operative intervention due to dystocia. In sports medicine, it is known that lactic acid can affect muscular performance but be decreased by bicarbonate given orally before physical activity. Main Outcome Measures: If an intake of bicarbonate, one hour before stimulation with oxytocin in cases with a high AFL value, changes the AFL levels and enhances delivery outcome in dystocic deliveries. Design: Randomized controlled trial

NCT ID: NCT04210908 Completed - Labor Long Clinical Trials

Biofeedback for Second Stage of Labor

Start date: April 30, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to examine whether transperineal ultrasound as visual biofeedback can be used during labor as an effective tool for shortening the second stage of labor and reducing the need for instrumental delivery, in a prospective randomized design.

NCT ID: NCT03856307 Completed - Clinical trials for Obstetric Complication

Reliability of Simple Sonographic Findings Acquired With Hand-held Apparatuses to Inform Obstetric Diagnosis

Start date: March 1, 2019
Phase:
Study type: Observational [Patient Registry]

the study aims to assess the reliability of ultrasound findings measured by hand held ultrasound probes used by operators with variable experience in a low resource hospital.