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Pregnancy clinical trials

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NCT ID: NCT01730170 Completed - Pregnancy Clinical Trials

Maternal Outcomes and Neurodevelopmental Effects of Antiepileptic Drugs (MONEAD)

MONEAD
Start date: January 2013
Phase:
Study type: Observational

Epilepsy is one of the most common neurological disorders affecting women of childbearing age. Poor pregnancy outcomes are increased in these women and their children. The proposed studies will increase our knowledge on multiple levels to improve care and reduce adverse outcomes in these mothers and children. An overall goal of this study is to establish the relationship between antiepileptic drug exposure and outcomes in the mother and child as well as describe and explain the variability in antiepileptic drug exposure and response.

NCT ID: NCT01727947 Completed - Pregnancy Clinical Trials

Influence of Sperm With Large Nuclear Vacuole on ICSI Outcomes

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

Current research on sperm morphology has been directed towards the dysmorphisms of the sperm head. A new technique based on the motile sperm organelle morphology examination (MSOME) allows the detection of sperm with large nuclear vacuoles (SLV). Large nuclear vacuoles are specific sperm alterations observed under high magnification, and their presence has been related to increased DNA fragmentation and denaturation.

NCT ID: NCT01720004 Completed - Clinical trials for Pregnancy, Childbirth and the Puerperium

A Pilot Randomized Controlled Trial of Repeated Hands-and-Knees Positioning During Labour

LPT2
Start date: October 2010
Phase: Phase 1
Study type: Interventional

The investigators designed a pilot randomized controlled trial to assess the feasibility and acceptability of repeated hands-and-knees positioning during labour. The objectives were 1) to provide an estimate of enrollment rates, 2) to assess compliance with the study protocol by participants and care providers, 3) to obtain women's views about their experiences using the hands-and-knees position, and 4) to provide estimates of treatment effects to inform the sample size calculation for a large trial.

NCT ID: NCT01718236 Completed - Pregnancy Clinical Trials

Modern Myorelaxation Procedure and Reversal of Neuromuscular Blockade With General Anesthesia for Caesarean Section

RocSugIO
Start date: September 2012
Phase: Phase 4
Study type: Interventional

The project aims to introduce into clinical practice for Caesarean section conducted under general anesthesia with the rapid induction myorelaxation with rocuronium and the reversal of neuromuscular blockade by using sugammadex. The aim is to demonstrate at least the same efficiency and confirm the safety of the procedure for both mother and newborn compared with older procedure.

NCT ID: NCT01708018 Completed - Pregnancy Clinical Trials

Effects of Relaxing Hydrotherapy in Third Trimester of Pregnancy

Start date: July 2012
Phase: N/A
Study type: Interventional

This study will be the first scientific approach to investigate physical and psychological effects of the passive hydrotherapy-method WATSU (WaterShiatsu) on women and their unborn children at the third trimester of pregnancy. Potential therapeutic benefits of the method shall be evaluated. It is being hypothesized that WATSU is related to measurable changes in everyday stress perception, psychological wellbeing, quality of life, pregnancy-related low back pain, tonus of the uterus, amount of amniotic fluid, spontaneous course of breech presentations, prospects of external cephalic versions. Participants in the intervention-group will be treated twice with WATSU (60 minutes per treatment, standardized sequence) in the >36th week of pregnancy. There will not be any sham-intervention in the control-group. Both groups will be examined by ultrasound (prior and after the treatments plus on day 8 of the trial) and answer questionnaires (prior and after the treatments plus once a week until birth).

NCT ID: NCT01707784 Completed - Pregnancy Clinical Trials

Effects of Stress on Glucose Tolerance During Pregnancy

Start date: October 2012
Phase:
Study type: Observational

The objective of the study is to investigate the effect of stress on glucose tolerance during pregnancy. The main objectives of the study are to investigate if various measures of stress (stressful life events, the perceived level of stress and the cortisol or copeptin concentrations) differ between pregnant women with and without gestational diabetes during the end of the second/beginning of the third trimester when presenting for their routine glucose tolerance testing. Secondary objectives are the link between these different stress measures and the routinely measured fasting and stimulated glucose levels during the oral glucose tolerance test.

NCT ID: NCT01700374 Completed - Pregnancy Clinical Trials

Happy Mommy! Happy Baby! Study

FAP
Start date: August 2012
Phase:
Study type: Observational

The purpose of this study is to determine how difficult life-events that women experienced during their childhood might affect their babies. Women who are asked to participate in this study will fill out forms about their physical and mental health, have 3D ultrasounds of their baby's adrenal gland, have their stress responses measured and have their baby's development and stress responses assessed.

NCT ID: NCT01699243 Completed - Anesthesia Clinical Trials

Continuous Noninvasive Method for Estimating and Predicting Maternal and Fetal Hemodynamic Changes During Regional Anesthesia

Start date: September 1, 2012
Phase:
Study type: Observational

Machine learning techniques and algorithms originally developed for use in the field of robotics can be applied to continuous, noninvasive physiological waveform data to discover hidden, hemodynamic relationships. Newly developed algorithms can, in real-time: 1) predict cardiovascular collapse well ahead of any clinically significant changes in standard vital signs, 2) monitor and estimate fluid resuscitation needs, 3) estimate acute blood loss volume, and 4) estimate intracranial pressure. The investigators hypothesize that these same methods can be used to predict functional hypovolemia during regional anesthesia for labor or fetal intervention.

NCT ID: NCT01698346 Completed - Pregnancy Clinical Trials

Pertussis (Tdap) Vaccination in Pregnancy

Start date: February 2012
Phase: Phase 4
Study type: Interventional

Despite good vaccination coverage, included in national immunization programs in developed countries, the number of reported pertussis cases is rising, also in very young infants. Current immunization strategies fail to protect infants too young to be immunized with the licensed vaccine. Different strategies are possible to close the gap of susceptibility between the loss of maternal antibodies and protection by vaccination. The main aim of the present study is to measure the influence of an adult pertussis booster in pregnant women, on the titer and duration of maternal antibodies in their infants. Early humoral immunity will be assessed and the influence on vaccine response of the infant measured. The present study offers the opportunity to have new insights in neonatal immunological mechanisms against pertussis and a better understanding in strategies to protect infants against pertussis.

NCT ID: NCT01697683 Completed - Clinical trials for Pregnant Women Who Test Positive for Bacterial Vaginosis

Probiotic Therapy for the Reversal of Bacterial Vaginosis in Pregnancy

ProVIP
Start date: May 2012
Phase: Phase 2
Study type: Interventional

This study will add to the current knowledge and literature on the ability of an oral lactobacilli preparation to return the vaginal flora to a normal state in pregnant women. The results will potentially serve as the basis for a multi-centre Phase III randomized clinical trial to determine the efficacy of this treatment in preventing preterm birth.