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Pregnancy clinical trials

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NCT ID: NCT02408315 Completed - Pregnancy Clinical Trials

Induction With Misoprostol: Oral Mucosa Versus Vaginal Epithelium (IMPROVE)

IMPROVE
Start date: September 2015
Phase: Phase 3
Study type: Interventional

The primary objective of this study is to compare the efficacy and safety of vaginal and buccal misoprostol for women undergoing labor induction at greater than or equal to 37+ 0 completed weeks gestation. Thus, the investigators have both efficacy and a safety primary outcomes. The secondary objective of this study is to assess the pharmacokinetic(PK) parameters with these two routes of administration in a sub-cohort of this trial. The long term objective of this line of research is to inform providers' clinical decision making for the large number of women having labor induction. By providing robust PK and pharmacodynamic (PD) evaluation, clinical outcomes data for these two routes of administration, clinicians will be informed for evidence-based decisions about the preferred route of administration of misoprostol.

NCT ID: NCT02402855 Completed - Pregnancy Clinical Trials

NAITRE (PreNAtal Care in deprIvaTed enviRonnEment)

Start date: June 7, 2016
Phase: N/A
Study type: Interventional

This study aims to evaluate the impact of financial support on improving the management of prenatal care in pregnant women with low incomes. The judgment criterion is clinically pertinent: complications of pregnancy. This study also aims to evaluate attitudes to this approach through a qualitative survey. It is planned to include 4000 women distributed into two arms of 2000 each. One group will receive financial support (prepaid payment card credited for each consultation attended according to the scheduled follow-up as recommended by the Haute Autorité de Santé); the other group will not. The management of the pregnancy for both groups will not be modified.

NCT ID: NCT02399839 Terminated - Pregnancy Clinical Trials

Global Lomitapide Pregnancy Exposure Registry

Start date: October 2014
Phase:
Study type: Observational [Patient Registry]

To evaluate the outcomes of pregnancy in women treated with lomitapide.

NCT ID: NCT02398565 Completed - Pregnancy Clinical Trials

Pregnancy Subsequent to Ventral Hernia Repair

Start date: March 2015
Phase: N/A
Study type: Observational

We will examine the outcome of ventral hernia repair with subsequent pregnancy

NCT ID: NCT02397291 Terminated - Pregnancy Clinical Trials

Transplacental Gradients and Transport in Intrauterine Growth Restricted (IUGR) Pregnancies Compared to Normal Pregnancies.

Start date: January 2001
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the transplacental gradients for 6 polyols and mannose are altered in intrauterine growth restricted (IUGR) pregnancies compared to normal pregnancies and b) to determine the relative contributions of transplacental transport vs production by the conceptus of both inositol (the major polyol) and mannose in IUGR and normal pregnancies using stable isotopic methodology.

NCT ID: NCT02395081 Completed - Pregnancy Clinical Trials

Trial of Vitamin D Supplements to Raise Calcidiol Levels of Pregnant Women in Mongolia

Start date: February 2015
Phase: N/A
Study type: Interventional

A double-blind randomized, placebo-controlled trial comparing the impact of 600 IU, 2000 IU, or 4000 IU of Vitamin D3 on third trimester 25(OH)D levels and change from baseline. The Vitamin D will be integrated in a standard prenatal vitamin, which will be taken from 12-16 weeks' gestation and continue throughout pregnancy. Umbilical cord 25(OH)D levels will also be determined. The investigators will generate preliminary data regarding Vitamin D intake and hypertensive disorders, blood pressure, and arterial function measured by tonography. The investigators will independently test blood pressure and proteinuria to identify preeclampsia cases.

NCT ID: NCT02394574 Active, not recruiting - Pregnancy Clinical Trials

Household Air Pollution and Pregnancy Outcome

HAP
Start date: September 2012
Phase: N/A
Study type: Interventional

Exposure to Household air pollution (HAP) from burning biomass fuels is responsible for an estimated 2.5 million premature deaths and 3.7% of the loss of disability-adjusted life years (DALY) every year in developing countries.52-54 Of all environmental risks, such as unsafe water, poor sanitation, climate change and lead exposure, HAP accounts for the most mortality and DALY.55 Despite the magnitude of the problems associated with HAP, research on its health effects has been hindered by lack of accurate data on exposure and health outcomes. There are few studies available that report HAP exposures and development of adverse pregnancy outcomes from households using biomass fuels.

NCT ID: NCT02393144 Recruiting - Pregnancy Clinical Trials

Analysis of Contemporary Labor Patterns Measured Via Transperineal Ultrasonography

Start date: February 2015
Phase: N/A
Study type: Interventional

Primary aim of this study is to analyse contemporary labor patterns by measuring rate of dilatation and head descent via transperineal ultrasonography. Labor curves will be generated using data regarding rate of dilatation, head-descent obtained via transperineal ultrasonography. Factors which are known to effect duration of labor will be taken into account.

NCT ID: NCT02392741 Not yet recruiting - Obesity Clinical Trials

Effects of a Physical Exercise Program on Microcirculation and Pregnancy Outcomes in Obese Pregnant Women

Start date: March 2015
Phase: N/A
Study type: Interventional

This study aims to determine the effect of a physical exercise program on microcirculation and maternal and perinatal outcomes in obese women. A randomized clinical trial will be performed at IMIP with obese pregnant women assisted at the Instituto de Medicina Integral Professor Fernando Figueira (IMIP) prenatal service.

NCT ID: NCT02391870 Completed - Depression Clinical Trials

The Staying Well Study: An Open Trial of Mindfulness-Based Cognitive Therapy for the Prevention of Perinatal Depression

Start date: November 2008
Phase: N/A
Study type: Interventional

Pregnant women with histories of depression are at high risk of depressive relapse during the perinatal period, and options for relapse prevention are limited. Mindfulness-based cognitive therapy (MBCT) has strong evidence among general populations but has not been studied among at risk pregnant women. This study is the first phase of a multi-phase project adapting MBCT for perinatal women (MBCT-PD). It is being conducted in a collaboration between the University of Colorado, Emory University, and Kaiser Permanente at Colorado and Georgia.