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Labor Complication clinical trials

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NCT ID: NCT06420453 Completed - Labor Complication Clinical Trials

How Long Can Labor Last? Person Centred Care During Labor to Increase Safety for Women and Newborn

Start date: January 1, 2008
Phase:
Study type: Observational [Patient Registry]

"How long will my labor last" is a very common question for midwives who care for women during birth. To evaluate safe labor duration largely determines management and care during birth. Today a standardized tool is used by midwives to evaluate normal and safe labor called the partograph. The World Health Organization partograph is a decision-making support tool designed to assist midwives in identifying normal labor duration and women at risk of developing complications. The tool guide the use of care interventions intended to mitigate any perceived risks. The partograph has been in use since the 1950ies and has had a profound impact on care and management during labor. Normal labor progression according to the partograph is a linear progression with cervical dilation of 1 centimeter per hour (alert line) and any deviation from this should lead to an intervention.The purpose of this research project is to increase person-centred care during labor. Specifically, we want to provide updated comprehensive information on labor duration and patient safety for reduction of; unnecessary medical interventions during normal labor; morbidity and mortality in the new-born; maternal complications during delivery and the puerperal period.

NCT ID: NCT06371742 Completed - Labor Complication Clinical Trials

Study of the Fluid Intake Effect During Labour

Start date: February 1, 2017
Phase:
Study type: Observational

Ingestion during labor is an issue that has attracted the attention of the scientific community in recent decades, with different practices occurring in different countries. However, the scientific evidence of the risk / benefit of fluid intake in labor is still not fully understood. The aim of this study was to contribute with data that allow the evaluation of an eventual relationship between the amount of fluid ingested during labor and the type of delivery, the duration of labor, the occurrence of nausea and vomiting and the value of the Index of Apgar at the 1st and 5th minutes of the newborn's life. An observational study, with a convenience sample of 144 parturient from two hospitals of Portugal were employed. The analysis was based on recording the before mentioned variables and potentially confounding variables. In order to control for potential sources of bias in the study and to guarantee the homogeneity of the sample in the specific statistical treatment of each dependent variable, an observation grid was drawn up for all the participants in the study. Twenty eight of the parturient, the parturient's ambulation, labour analgesia, food intake during labour, the use of oxytocin during labour, the occurrence of postpartum complications, the birth weight of the newborn and the occurrence of birth complications.

NCT ID: NCT05339399 Completed - Labor Complication Clinical Trials

4 Versus 6 cm Active Phase of Labour

Start date: May 1, 2021
Phase:
Study type: Observational

A study to compare maternal and perinatal outcome between 4 and 6 cm cervical dilatation at amniotomy.

NCT ID: NCT04823598 Completed - Labor Complication Clinical Trials

Pushing and Manual Perineal Protection Techniques

Start date: April 21, 2021
Phase: N/A
Study type: Interventional

Perineal trauma during vaginal delivery is very common, especially in countries with a high prevalence of episiotomy. Perineal traumas can range from tears limited to the skin, subcutaneous and vaginal mucosa to severe tears involving the anal sphincter and rectal mucosa. Perineal trauma is associated with short-term morbidities such as bleeding, infection, pain, edema. Besides, it may cause long-term morbidities such as urinary incontinence, fecal incontinence, dyspareunia, a decrease in quality of life, a need for surgery, and psychosocial problems. Moreover, it is associated with an increase in national healthcare costs and malpractice cases. For these reasons, some measures to reduce the frequency of perineal trauma have been discussed for many years. Pushing techniques applied in the second stage of labor and manual perineum protection techniques applied during fetal expulsion are among these. Current data are insufficient to make definitive recommendations. In this study, it was aimed to compare different pushing and perineal protection techniques in the second stage of labor.

NCT ID: NCT04651309 Completed - Pregnancy Related Clinical Trials

Assessment of Labour Progress by Intrapartum Ultrasound

Start date: August 27, 2019
Phase: N/A
Study type: Interventional

Assessment of labor progress via digital exams is considered the standard of care in most delivery rooms. However, this method can be stressful, painful and imprecise and multiple exams increase the risk for chorioamnionitis. Trans-perineal ultrasound (TPUS) was found to be an objective noninvasive way to monitor labor progress. The study aim is to investigate whether, in nulliparous women, the use of TPUS during labor can reduce the number of vaginal exams and the incidence of chorioamnionitis.

NCT ID: NCT04413890 Completed - Labor Complication Clinical Trials

Comparison of Two Rhythm of Administration of Prostaglandin Gel for Induction of Labor

GELFREQ
Start date: December 17, 2019
Phase: Phase 2
Study type: Interventional

The study compares two rhythms of administration of prostaglandin vaginal gels for cervical priming before induction of labor in term patients. In our institution, prostaglandin gels are given for a maximum of three times, with induction by oxytocin and amniotomy the day after the last gel whatever Bishop score has been obtained. This management results in some patient spending four days in hospital before delivery. The aim of the study is to compare our classical management scheme with a reduced interval between to gels, of 12h instead of 24 h. The primary outcome will be the time elapsed between the first prostaglandin gel and delivery. Tolerance of both management patterns will also be evaluated through a satisfaction survey.

NCT ID: NCT03752879 Completed - Labor Complication Clinical Trials

The Association Between Kristeller Maneuver and Pelvic Floor Trauma After Vaginal Delivery

Start date: May 18, 2019
Phase:
Study type: Observational

We want to investigate the association between fundal pressure in the second stage and the risk of levator ani muscle (LAM) injury.

NCT ID: NCT03342508 Completed - Labor Complication Clinical Trials

Fetal Pillow Randomized Controlled Trial

Start date: January 13, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate outcomes following cesarean delivery for failure to progress with the use of the Fetal Pillow. Our hypothesis is that time to delivery of the fetus is shorter with implementation of the Fetal Pillow.

NCT ID: NCT03276117 Completed - Labor Pain Clinical Trials

Wide Use of Paperless Partograph in Evaluation of Labour

labourRecord
Start date: February 2, 2017
Phase: N/A
Study type: Observational

Paperless partograph wide using in labour room as simple tool in evaluation of labour