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Pregnancy clinical trials

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NCT ID: NCT01708239 Recruiting - Pregnancy Clinical Trials

Left Rule, D-Dimer Measurement and Complete Ultrasonography to Rule Out Deep Vein Thrombosis During Pregnancy.

Start date: October 2012
Phase:
Study type: Observational

In pregnant women with suspected DVT, a sure diagnosis is mandatory. In non-pregnant patients, sequential diagnostic strategies based on 1) the assessment of clinical probability, 2) D-dimer measurement and 3) compression ultrasonography (CUS) have been well validated. Clinical probability assessment by clinical prediction rules (CPRs) is a crucial step in the management of suspected DVT. However, the most commonly used CPR for DVT, the Wells' score, has never been validated in pregnant women. Recently, the 'LEFt' clinical prediction rule was derived and internally validated. A prospective validation of this rule is now warranted, and we plan to use it in our prospective study. The second step used in the diagnostic strategy including non-pregnant patients is D-dimer measurement. The test has been widely validated in non-pregnant patients and, in association with a non-high clinical probability, it allows to safely rule out DVT. As D-dimer level raise steadily during pregnancy, the specificity of the test decreases and it is less useful in pregnant women. Data from the literature clearly suggest that the usual cut-off set a 500 ng/ml would safely rule out DVT in pregnant women [6]. As the usual cut-off has never been prospectively validated in pregnant women with suspected DVT, we would like to use it in our study. Some studies suggested that complete CUS is safe to rule out DVT in pregnant women. However, this test is not always available. Therefore, a strategy in which the association of clinical probability assessment and D-dimer measurement would allow to safely rule out DVT in a significant proportion of patients without performing a complete CUS, would be of great help in everyday clinical practice and would probably be cost-effective. Therefore, we plan a prospective study to assess the safety of a sequential diagnostic strategy based on the assessment of clinical probability with the LEFt rule, D-dimer measurement and complete CUS in pregnant women with suspected DVT.

NCT ID: NCT01696201 Recruiting - Pregnancy Clinical Trials

Effect of Physical Exercise Program on Outcomes and Level of Depression

Start date: October 2009
Phase: N/A
Study type: Interventional

Due to physical and physiological changes that occur in pregnant women, depression is very common during this period. Recent research findings indicate that antenatal maternal mood state impacts on babies health. Nowadays, many researchers are focussed on examining the effects of physical exercise on foetal and maternal outcomes. The main aim of this study was to assess the effectiveness of a supervised exercise program consisted of 25-30 minutes of cardiovascular exercise,10 minutes of specific exercises (strength and balance exercises), and 10 minutes of pelvis floor muscles training, on the prevention and treatment of depression in pregnant women. Additionally, the other purpose of the study was to analyze the effects of depression and physical exercise on outcomes. Hypothesis: Pregnant women who do regular exercise during their pregnancies would have a better mood state than pregnant women who are sedentary, without having any negative effect on outcomes.

NCT ID: NCT01675180 Recruiting - Pregnancy Clinical Trials

Self Reported Oral Health, Awareness and Attitude Towards Dental Care Among Pregnant Women

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

Purpose/Objective of the study: The main objective of the study is to investigate oral health awareness and attitudes towards oral health among Norwegian pregnant women and assess the impact of information about oral hygiene on the risk of dental caries during pregnancy. The hypothesis of the study are: 1. The state of oral health during pregnancy depends on pregnant woman's preventive oral hygiene behaviour and practice. 2. Pregnant women with high level of oral health awareness and positive attitude towards oral health are more likely to visit their dentists regularly and have better oral hygiene compared to those with less awareness. 3. Proper information and guidance on oral hygiene care provided during pregnancy can help to improve oral bacteriological milieu and reduce the dental caries risk among pregnant women.

NCT ID: NCT01659749 Recruiting - Pregnancy Clinical Trials

Educational, Social Support, and Nutritional Interventions and Their Cumulative Effect on Pregnancy Outcomes and Quality of Life in Teen and Adult Women With Phenylketonuria

Start date: June 1995
Phase: N/A
Study type: Interventional

The purpose of this project is to study the effectiveness of teaching teens and young women with Phenylketonuria (PKU) or Maple Syrup Urine Disease (MSUD) about their disease and nutrition related issues in a camp environment. It will also look at pregnancy outcome results in women with PKU who attended Metabolic Camp and compare their results to other women with PKU who have not attended the Metabolic Camp.

NCT ID: NCT01636895 Recruiting - Clinical trials for Pregnancy Complications Parasitic

Evaluation of SP Resistance and Effectiveness of IPTp in Nigeria

OR1
Start date: January 2011
Phase: Phase 4
Study type: Interventional

The study has two components: component A is a cohort study to determine the in vivo efficacy of SP to clear and prevent malaria parasitaemia in asymptomatic pregnant women and component B is a cross sectional study of women delivering at the study hospitals to assess the effectiveness of SP-IPTp to reduce adverse maternal and birth outcomes in the current context of increasing SP resistance. Results of component A and B studies will be used to model the relationship between the prevalence of molecular markers of SP resistance, in vivo efficacy to clear parasite and the effectiveness of SP-IPTp and to develop guidelines for routine monitoring effectiveness of SP-IPTp as part of ANC surveillance.

NCT ID: NCT01610115 Recruiting - Pregnancy Clinical Trials

HBV DNA Levels During Pregnancy in Chronic Hepatitis B

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

To elucidate the natural course of chronic hepatitis B by serial HBV DNA and alanine aminotransferase (ALT) levels during pregnancy

NCT ID: NCT01605474 Recruiting - Pregnancy Clinical Trials

Patient Satisfaction of Cervical Ripening in an Outpatient Setting

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

This study examines whether outpatient pre-induction cervical ripening improves patient satisfaction and is safe and effective.

NCT ID: NCT01442584 Recruiting - Pregnancy Clinical Trials

Transplantation of Ovarian Cortex to Restore Fertility

ovatrspl
Start date: July 2011
Phase: N/A
Study type: Interventional

Ovarian transplantation has been shown to restore fertility.

NCT ID: NCT01345071 Recruiting - Clinical trials for Rheumatoid Arthritis

Preconceptional Counselling in Active Rheumatoid Arthritis

PreCARA
Start date: September 2011
Phase: N/A
Study type: Observational

The first objective of the study is to evaluate a treat to target treatment strategy in women with moderate to high disease activity of RA and a pregnancy wish, from pre-pregnancy. The treatment strategy is based on deliberate treatment decisions to lower disease activity, including the continuation or start of biological treatment (in particular anti-Tumor Necrosis Factor [anti-TNF]), based on a standard care protocol in the Erasmus MC. The second objective is to evaluate the safety of the use of anti-TNF during pregnancy among women with a rheumatic disease that require the use of anti-TNF before or during pregnancy.

NCT ID: NCT01287273 Recruiting - Pregnancy Clinical Trials

The Impact of Early Embryos Incubation on Pregnancy Rate in IVF

IVF-2010
Start date: April 2011
Phase: N/A
Study type: Observational

Frozen- thawed embryos obtained by IVF treatments are transferred to the uterus immediately following thawing or after incubation for additional 24-72 hours. The two methods are routine in IVF laboratories. In this study the investigators would like to compare between these two methods in terms of implantation rate, pregnancy rate and delivery.