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Pregnancy clinical trials

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NCT ID: NCT00809666 Completed - Hypertension Clinical Trials

Measuring Blood Pressure in Pregnancy Using Mercury and Automated Device

PRAM
Start date: May 2000
Phase: N/A
Study type: Interventional

The aim of the PRAM study was to determine whether women diagnosed with hypertension in pregnancy, using the traditional mercury device, have the same pregnancy outcomes when blood pressure is measured by either an automated device or a mercury device throughout the pregnancy.

NCT ID: NCT00804765 Completed - Obesity Clinical Trials

Impact of Education During Pregnancy in Overweight Pregnant Women

ETOIG
Start date: September 2008
Phase: N/A
Study type: Interventional

Metabolic environment of the foetus during pregnancy in obese women is altered and the child exposed at an increased risk of obesity. Rapid infancy and childhood weight gain is associated with subsequent obesity. The purpose of the study is to test the efficacy of an educational intervention during pregnancy in obese or overweight women, on the reduction of rapid infancy weight gain in the two first years of life.

NCT ID: NCT00799500 Completed - Pregnancy Clinical Trials

Bacterial Vaginosis in Pregnancy: Detection by Weekly Vaginal pH Testing

Start date: January 2007
Phase: N/A
Study type: Interventional

Interventional study to assess the effect of early detection and treatment of bacterial vaginosis in pregnancy on preterm delivery rate.

NCT ID: NCT00795561 Completed - Pregnancy Clinical Trials

Management of Nausea and Vomiting of Pregnancy

DIM
Start date: April 2009
Phase: N/A
Study type: Interventional

Upto 80% of all pregnant women experience some form of nausea and vomiting (NVP) during their pregnancy. Hyperemesis gravidarum, a more severe form of NVP affects approximately 0.3- 2.0% of pregnancies and is the commonest indication for admission to hospital in the first half of pregnancy and second only to preterm labor as a cause of hospitalization overall. According to the Hyperemesis Education and Research Foundation, conservative estimates indicate that HG can cost a minimum of $200 million annually in house hospitalizations in the United States of America. The investigators aim to conduct a randomized controlled trial to test the hypothesis that the availability of day care services for the initial treatment of NVP reduces the mean duration of stay in hospital by 1 day and results in significantly greater patient satisfaction compared with standard inpatient management.

NCT ID: NCT00783770 Completed - Pregnancy Clinical Trials

Maternal and Infant Cord Blood Monosaccharide Content

Start date: July 2005
Phase: N/A
Study type: Observational

Mother's breast milk provides many benefits to babies with regard to development and improved health. We believe the simple sugars which make up these complex sugars in breast milk and are also found in the brain may be critical to normal brain development in term and preterm infants. Babies are exposed to these sugars by placental transport during pregnancy and through mother's breast milk after they are born. For the preterm infant, we do not know if breast milk gives enough of these sugars compared to what the baby gets during pregnancy. A maternal blood sample and blood samples from the baby's umbilical cord will provide us with background information for developing a supplement of special sugars that can be added to infant formulas to provide the amount that the baby usually gets during pregnancy and from breast milk.

NCT ID: NCT00782730 Completed - Pregnancy Clinical Trials

Assessment of Third Trimester Post-void Residual and Validation of Bladder Scanner in Pregnancy and Post-partum

Start date: October 2008
Phase: N/A
Study type: Observational

This will be a descriptive study measuring the post—void residual of patients in the third trimester and postpartum. Also, bladder scan values will be compared to the amount of urine obtained from a Foley catheter to determine the accuracy of the bladder scanner in the third trimester and postpartum.

NCT ID: NCT00774124 Completed - Diabetes Mellitus Clinical Trials

Improving Outcomes in Underserved Women With GDM

Start date: August 2007
Phase: N/A
Study type: Interventional

Our objective is to test an innovative approach to improve outcomes among underserved women with gestational diabetes. We ill utilize a multi-lingual, Interactive Voice Response (IVR) -enabled telephone system to facilitate diabetes control and thereby improve pregnancy outcomes. Our hypothesis is that Telemonitoring will improve maternal glycemia, thereby reducing infant birth weights and leading to improved pregnancy outcomes.

NCT ID: NCT00766818 Completed - HIV Clinical Trials

The Effect of Pregnancy on the Pharmacokinetics of the Kaletra Tablet

Start date: January 2007
Phase: Phase 1
Study type: Interventional

In this study, we are looking at blood concentrations of Kaletra in HIV positive patients during pregnancy. The patients will come in for 4 visits lasting ~24hrs. These visits take place at 20-24 weeks, 30 weeks, 32 weeks and 8 weeks post-partum. At the end of vist 2 (week 30), we will increase your dose to 2 adult Kaletra tablets, and one pediatric Kaletra tablet (total dose 500/125mg). The dose will remain increased until you are 2 weeks post partum, then it will return to the standard 2 adult tablets (400/100mg).

NCT ID: NCT00763672 Completed - Hypertension Clinical Trials

MorbiMortality Amelioration in Preeclamptic Primiparas Study. MoMA Pre Prim Study

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

The purpose of this study is to determine whether close monitoring of patients with a high sFlt1 plasma level between 25 and 28 weeks of gestation (i.e. at high risk of subsequent preeclampsia) improves maternal and fetal outcomes. The investigator hypothesize that 1/ early screening for preeclampsia by plasmatic sFlt1 will reduce maternal and fetal mortality and morbidity and 2/ a simple urinary PlGF screening will be effective.

NCT ID: NCT00741312 Completed - Pregnancy Clinical Trials

Influence of Physical Exercise on Endothelial Function in Pregnant Women

Start date: October 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine the effect of regular aerobic exercise on endothelial function in pregnancy.