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Pregnancy clinical trials

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NCT ID: NCT02692404 Completed - Pain Clinical Trials

Labor Pain and Postpartum Behavioral Health Outcomes Study

LPPD
Start date: January 2016
Phase:
Study type: Observational

In this pilot prospective longitudinal observational study, women who are pregnant and who will be experiencing childbirth for the first time will be recruited at the third trimester and observed longitudinally for psychiatric and pain characteristics until 3 months postpartum. The primary outcome is postpartum depression, assessed by Edinburgh Postnatal Depression Scale (EPDS). Infants will also be observed for infant development characteristics over time. Women who choose to receive labor epidural analgesia will be observed, as well as women who choose to avoid labor epidural analgesia. At baseline, women will complete baseline surveys as well as a baseline pain sensitivity test (quantitative sensory testing, QST). During labor, they will complete an electronic pain diary delivered by a bedside mobile device. Three postpartum assessments will occur over 3 months to assess maternal depression, other psychosocial variables, and infant development.

NCT ID: NCT02691884 Not yet recruiting - Pregnancy Clinical Trials

The Effect of Pressure Exerted on the Maternal Abdominal Wall by the Ultrasound Probe on Fetal Heart Rate

Start date: March 2016
Phase: N/A
Study type: Observational

The aim of the study is to assess the change of fetal heart rate in response to the amount of pressure exerted on the maternal abdomen. The amount of pressure will be quantified using an electronic pressure sensor (FSR 400- Round Force Sensor, Interlink).

NCT ID: NCT02691364 Not yet recruiting - Pregnancy Clinical Trials

Different Regulation of Immune Cells in Patients With Preeclampsia

Start date: April 2016
Phase: N/A
Study type: Observational

Adaptation of the maternal immune system to accommodate the semi-allogeneic fetus is necessary for pregnancy success. Dysregulation of this immune adaptation is implicated in reproductive disorders as infertility, recurrent miscarriage, fetal growth restriction, and preeclampsia. The mechanisms being responsible for fetal tolerance are not known. Several T cell subsets have been implicated in fetal tolerance. The effects of preeclampsia on memory cells are not known. The main objective of this study is to analyze the effect of preeclampsia on levels of immune cells.

NCT ID: NCT02689739 Withdrawn - Pregnancy Clinical Trials

Validation of Ultrasound in Predicting a Low Lying Placenta Throughout Pregnancy

Start date: July 1, 2015
Phase:
Study type: Observational

This is a prospective observational study comparing venous Doppler flow in the lower extremities of pregnant women. Pregnant women with a BMI >/= 30 will be compared to those with a BMI < 30.

NCT ID: NCT02683005 Completed - Pregnancy Clinical Trials

Study of Hepatitis C Treatment During Pregnancy

HIP
Start date: September 2016
Phase: Phase 1
Study type: Interventional

Sofosbuvir and ledipasvir (LDV/SOF) are new directly acting antiviral drugs for the treatment of hepatitis C (HCV) that are highly effective, orally administered, well tolerated and preclinical evaluations in animal models indicate safe administration during pregnancy. This project will evaluate the safety and pharmacokinetics of antenatal LDV/SOF treatment for 12 weeks during the second and third trimester. If proven to be effective, antenatal treatment of HCV with LDV/SOF will prevent maternal HCV-related liver disease, perinatal transmission of HCV, and community transmission of HCV.

NCT ID: NCT02677558 Completed - Obesity Clinical Trials

The Impact of Obesity on Cardiac Function in Pregnancy

CFOP
Start date: January 2016
Phase:
Study type: Observational

The purpose of this study is to determine the impact of obesity in pregnancy on maternal cardiac function. For this, morbidly obese term pregnant women (study group) and term pregnant women of normal weight are assessed by transthoracic echocardiography.

NCT ID: NCT02676882 Completed - Pregnancy Clinical Trials

EnBrace HR for Depression Treatment and Prevention in Women Trying to Conceive and Early Pregnancy

Start date: January 24, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the effectiveness of the EnBrace HR prenatal supplement in preventing depression in women with a history of depression who have decided to stop taking antidepressants during their pregnancy, or treating women who are currently in a depressive episode while pregnant or planning pregnancy.

NCT ID: NCT02675595 Recruiting - Pregnancy Clinical Trials

5D Versus Conventional 2D Fetal Echocardiography During Second Trimester of Pregnancy

Start date: January 2016
Phase: N/A
Study type: Observational [Patient Registry]

Hypothesis: In Women in the second trimester of pregnancy 5D offers an alternative method for fetal Echocardiography compared to conventional 2D scanning Question: Does 5D software technology is as efficient as 2D scanning in fetal echocardiography of second trimesteric fetuses? Aim: This study aims at assessing the accuracy of performance of the 5D as a new scanning technology in fetal Echocardiography compared to the conventional use of 2D scanning.

NCT ID: NCT02675179 Completed - Pregnancy Clinical Trials

EOS® Versus Spiral CT Technique for Achieving a Pelvimetry in Suites of Obstructed Labor.

PELVI-EOS
Start date: May 27, 2016
Phase: N/A
Study type: Interventional

The aim of this study is to demonstrate in vivo the concordance of the imagery system EOS and the spiral CT in women having had an obstructed delivery. If this concordance is demonstrated, it would allow the use of this new technique of imagery, to realize a pelvimetry during the pregnancy less irradiating for the mother, and the fetus.

NCT ID: NCT02674022 Completed - Pregnancy Clinical Trials

Screening for Metabolic Problems in Mothers of Children With Autism and Typically Developing Children

Start date: January 20, 2016
Phase: N/A
Study type: Interventional

The purpose of this research study is to screen for metabolic abnormalities that are maternal risk factors for having a child with autism.