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Pregnancy clinical trials

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NCT ID: NCT02283606 Not yet recruiting - Pregnancy Clinical Trials

Sonoelastography of the Uterine Cervix Before Induction of Labor

SUCI
Start date: November 2015
Phase: N/A
Study type: Observational

The investigators aim to measure sonoelastographically the elasticity of the uterine cervix in pregnant patients at term before induction of labor and compare between patients with successful and failed inductions.

NCT ID: NCT02283567 Not yet recruiting - Pregnancy Clinical Trials

The Difference Between Elasticity of the Uterine Cervix in Singleton and Twin Pregnancies

DEU
Start date: November 2015
Phase: N/A
Study type: Observational

The investigators aim to compare elasticity of the uterine cervix in singleton and twin pregnancies of similar gestational age.

NCT ID: NCT02282475 Completed - Obesity Clinical Trials

Role of Liver and Visceral Fat in Glucose and Lipid Metabolism During Pregnancy

Start date: November 30, 2014
Phase:
Study type: Observational

Obesity, increased abdominal fat, fat stored in the liver, and insulin resistance may all be associated with adverse maternal and fetal pregnancy outcomes. This study will examine how fat storage changes during pregnancy; and if how the body stores fat impacts one's ability to metabolize glucose (sugar) during pregnancy.

NCT ID: NCT02277782 Terminated - Pregnancy Clinical Trials

Intrathecal Hydromorphone for Labor Analgesia

LITH
Start date: September 1, 2015
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the effect of intrathecal hydromorphone on the duration of labor analgesia and the incidence of epidural-associated temperature increase in laboring parturients. We hypothesize that intrathecal administration of longer-acting hydromorphone will: 1. Prolong the duration and improve the quality of analgesia in labor, and 2. Decrease the incidence of epidural-associated temperature increase in labor.

NCT ID: NCT02275897 Completed - Pregnancy Clinical Trials

Effect of Different Injection Speeds for Spinal Anaesthesia in Caesarean Section

Start date: March 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate if prolonging the speed of injection during spinal anaesthesia can reduce the incidence of hypotension and/or medication requirements thereby making it safer for the mother and foetus.

NCT ID: NCT02275442 Active, not recruiting - Pregnancy Clinical Trials

Effect of Precariousness in RUral Areas During preGNANCY

PRUGNANCY
Start date: September 2014
Phase: N/A
Study type: Observational

The link between precarious situations and health conditions are more described in previous study. Precarious situations are more frequent and complex especially in rural areas. There are recognized like a risk factor of complications during pregnancy and delivery. It's necessary to describe antenatal cares for rural women in precarious situations to prevent those situations, to understand their difficulties in order to reduce inequalities and health spending. The aim of the PRUGNANCY study is to understand the difficulties of rural parturient women and the strategies developed to overcome them. Recognized earlier precarious situations and valorized General Practitioners and restore them to the follow-up or parturient women.

NCT ID: NCT02273297 Recruiting - Obesity Clinical Trials

Healthy Start: Exploring the Fuel-mediated Programming of Neonatal Growth

Start date: July 2009
Phase:
Study type: Observational

The purpose of this study is to establish and follow longitudinally a cohort of ethnically diverse pregnant women and their offspring, in order to explore the hypothesis that fetal over-nutrition is associated with obesity, metabolic, and cardiovascular abnormalities in the offspring.

NCT ID: NCT02270801 Recruiting - Pregnancy Clinical Trials

Recombinant Human Thrombopoietin (rhTPO) in Management of Immune Thrombocytopenia (ITP) in Pregnancy

Start date: October 2014
Phase: Phase 3
Study type: Interventional

This clinical trial is undertaking by Qilu Hospital of Shandong University, aims at evaluating efficacy and safety of rhTPO in management of ITP in pregnancy.

NCT ID: NCT02269462 Completed - HIV Clinical Trials

A Study to Evaluate the Effects of Genetic Factors on the Pharmacokinetics of Antiretroviral Drugs During Pregnancy and Lactation

Start date: December 2012
Phase: N/A
Study type: Observational

Mother-to-child transmission of HIV (MTCT) during pregnancy and breastfeeding is prevented with maternal antiretroviral drugs (ARV) and infant nevirapine post-exposure prophylaxis (PEP). However, the pharmacokinetics of certain ARVs is associated with marked inter-individual variability. This variability has been associated with single nucleotide polymorphisms (SNPs) in genes encoding metabolising enzymes, transporters and transcriptional regulators. Pregnancy is also associated with additional changes in pharmacokinetics. The resulting sub-therapeutic or supra-therapeutic drug exposures may have serious consequences for virological control, MTCT, emergence of drug resistance, and toxicity. Foetal and infant exposure to maternal ARV during pregnancy and breastfeeding is believed to play a role in the prevention of mother-to-child transmission of HIV (PMTCT). However, such exposures may also result in toxicity. For example, efavirenz is contraindicated in children less than 3 years old or 10kg but transferred to breastfed babies through breast milk. On the other hand, double exposure to nevirapine from breast milk and PEP may also predispose breastfed infants to nevirapine-associated toxicity. In the proposed study, the influence of selected SNPs in certain drug disposition genes on the pharmacokinetics of efavirenz and nevirapine during pregnancy and lactation, as well as the level of infant exposure to both drugs through breast milk, will be studied. Mathematical models will be developed to predict potential dose optimisation strategies during pregnancy, and to predict infant exposure to maternal drugs through breast milk.

NCT ID: NCT02268877 Completed - Pregnancy Clinical Trials

A Randomized Prospective Analysis of Time to Diagnosis and Length of Stay of Emergency Department Pelvic Ultrasonography

Start date: March 2013
Phase: N/A
Study type: Interventional

The goal of this project is to compare the efficiency of pelvic ultrasounds performed by emergency medicine residents and attending physicians to the efficiency of pelvic ultrasounds performed by the department of radiology.