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High Risk Pregnancy clinical trials

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NCT ID: NCT05495789 Completed - High Risk Pregnancy Clinical Trials

The Effect of Virtual Reality and Music in High-Risk Pregnants on Non-Stress Test

Start date: January 9, 2023
Phase: N/A
Study type: Interventional

Aim: The aim of this study is to determine the effects of virtual reality and listening to music during the NST procedure on NST parameters, anxiety and satisfaction in high-risk pregnant. Hypotheses H01 In the NST process, there is no difference between the NST parameters of the virtual reality group and the NST parameters of the control group. H02 In the NST procedure, there was no difference between the anxiety score of the virtual reality group and the anxiety score of the control group. H03 There is no difference between the satisfaction score of the group in which virtual reality was applied in the NST procedure and the satisfaction score of the control group. H04 In the NST process, there is no difference between the NST parameters of the group to which the virtual reality is applied and the NST parameters of the musical group. H05 In the NST procedure, there was no difference between the anxiety score of the group in which virtual reality was applied and the anxiety score of the music group. H06 In the NST process, there is no difference between the satisfaction score of the group to which the virtual reality was applied and the satisfaction score of the music group. H07 In NST operation, there is no difference between the NST parameters of the music group and the NST parameters of the control group. H08 In the NST procedure, there was no difference between the anxiety score of the music group and the anxiety score of the control group. H09 There is no difference between the satisfaction score of the music group and the satisfaction score of the control group in the NST procedure.

NCT ID: NCT05093647 Completed - Sexual Behavior Clinical Trials

Sexual Function Changes in High-Risk Pregnancies

Start date: April 15, 2021
Phase:
Study type: Observational [Patient Registry]

Sexual Function Changes in High-Risk Pregnancies

NCT ID: NCT05021289 Completed - High Risk Pregnancy Clinical Trials

Guided Imagery on the Perceived Stress Level in High-Risk Pregnancies

Start date: February 1, 2021
Phase: N/A
Study type: Interventional

This research was conducted to identify the effect of the practice of Guided Imagery on the perceived stress level in high-risk pregnancies.

NCT ID: NCT04492072 Completed - Cesarean Section Clinical Trials

Misoprostol With Mechanical Dilation Versus Oxytocin With Mechanical Dilation for High-risk Pregnancy Inductions

MODE
Start date: August 17, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to specifically investigate whether oxytocin and mechanical dilation decreases the rate of cesarean section compared to misoprostol and mechanical dilation for pregnancies at risk of fetal compromise

NCT ID: NCT04201951 Completed - Clinical trials for Postpartum Hemorrhage

Tranexamic Acid for the Prevention of Blood Loss in High Risk Delivered Women

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

Postpartum hemorrhage and its complications are very well known causes for maternal mortality .Uterine atony is the most common cause for postpartum hemorrhage

NCT ID: NCT04089176 Completed - Cesarean Section Clinical Trials

Carbetocin Versus Oxytocin for Prevention of Postcesarean Hemorrhage in Pregnancy With High Risk for PPH

Start date: February 1, 2019
Phase: Early Phase 1
Study type: Interventional

Objective: study efficacy of carbtocin versus oxytocin for prevention postpartum hemorrhage in high risk pregnancy who undergo cesarean section

NCT ID: NCT03772080 Completed - Prematurity Clinical Trials

Prematurity Education in High Risk Pregnancies

Start date: November 5, 2018
Phase: N/A
Study type: Interventional

Prematurity is associated with significant morbidity and mortality. Given the high risk of death and disability, it is important for parents to understand the complications of prematurity so they can make decisions for their child. Unfortunately, these discussions often occur in the acute setting of threatened preterm labor when stress and anxiety make comprehension difficult. This study aims to improve parental understanding by providing early education of prematurity in the clinic setting for patients at high risk of preterm delivery.

NCT ID: NCT03584763 Completed - High Risk Pregnancy Clinical Trials

Frequency of Performing Umbilical Artery Doppler in the Third Trimester in High Risk Pregnancy

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

The aim of the current study was to produce a high quality evidence on the best frequency of performing umbilical artery Doppler for high risk pregnant women in the third trimester.

NCT ID: NCT03522909 Completed - Communication Clinical Trials

The Center for Peripartum Optimization

Start date: January 2017
Phase:
Study type: Observational

In January 2017 investigators started a Center for Peripartum Optimization (CPO) with the aim of optimizing a patient's clinical status in an outpatient setting to minimize unnecessary laboratory tests and studies, costly inpatient consultations, the likelihood of post-surgical adverse events, escalations in level of care, inpatient admissions and readmissions. This research project seeks to evaluate the impact of this innovative concept on patient outcomes during the last 12 months. Investigators will accomplish this by collecting retrospective data from patients' electronic medical records in the intervention group and comparing it to data gathered from a controlled group of patients with similar comorbidities but who were not evaluated at the CPO clinic.

NCT ID: NCT03419065 Completed - High Risk Pregnancy Clinical Trials

Relaxation Interventions for Pre-term Mothers on Hospitalized Bed-Rest

Start date: January 1, 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effects of participation in relaxation exercises on pregnant women who are hospitalized on bed-rest.