Clinical Trials Logo

Pregnancy clinical trials

View clinical trials related to Pregnancy.

Filter by:

NCT ID: NCT01736826 Completed - Pregnancy Clinical Trials

Free DNA and Nucleosome Concentrations in Pathological Pregnancies

Start date: June 2015
Phase:
Study type: Observational

The primary objective of this study is to demonstrate that plasma concentrations of nucleosomes and free DNA differ between three groups: 1. pregnant patients with complications typical of placental insufficiency or venous thrombosis (group P), 2. healthy women (Group T1) and 3. healthy pregnant women (Group T2).

NCT ID: NCT01735695 Recruiting - Pregnancy Clinical Trials

Performance Evaluation Study for a New Meconium Detection Test

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

The purpose of this study is to collect amniotic fluid samples from pregnant women. Amniotic fluid samples will be tested for meconium with a new assay. The results will be correlated with other laboratory tests.

NCT ID: NCT01734655 Completed - Pregnancy Clinical Trials

Study of the Validity of Using the MEQ to Measure Mindful Eating in Pregnant Women

MEQ
Start date: November 2012
Phase: N/A
Study type: Observational

The Specific Aim of this supplemental project is to evaluate the Mindful Eating Questionnaire (MEQ) to determine if it is a valid instrument for pregnant women. During this project, the MEQ will be qualitatively evaluated in a sample of pregnant women who are similar in age, ethnicity, education, and marital status to the women targeted for recruitment in the parent study. The qualitative evaluation will include a focus group with 10 participants followed by 30 individual cognitive interviews. Comments from the interviews will be summarized and analyzed systematically for each of the 28 questions of the MEQ and the interviewer will use findings from initial interviews to inform subsequent interviews. Content validity will be evaluated based on responses from the focus group and cognitive interviews, and MEQ items will be evaluated for comprehension, retrieval, judgment, and response. Strengths, weaknesses, relevance, comprehensiveness, and interpretations will be reported for each of the MEQ questions. We will also have some of the more traditional validation parameters (the inclusion of other questionnaires) in the study to collect data on convergent and discriminant validity. The resulting publication will provide readers with a thorough report on the utility and appropriateness of using the MEQ to quantify mindful eating in pregnant women.

NCT ID: NCT01731639 Completed - Pregnancy Clinical Trials

Motile Sperm Organelle Morphology Examination (MSOME) Influence on Intracytoplasmic Sperm Injection (ICSI) Outcomes in Infertile Couples

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

A new technique based on the motile sperm organelle morphology examination (MSOME) at a magnification of at least ×6000 has been developed. The MSOME assesses the nucleus, for both shape and chromatin content, which is the most important sperm organelle in influencing intracytoplasmic sperm injection (ICSI) outcomes.

NCT ID: NCT01730963 Completed - Pregnancy Clinical Trials

Multi-Reader Multi-Case Study to Identify Uterine Contractions Recorded From Laboring and Nonlaboring Patients by Practicing Clinicians

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

This multi-reader multi-case study was designed to evaluate the performance of SureCALL® Labor Monitor® (SureCALL®) directly to the standard Tocodynamometer device (TOCO).

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: NCT01729533 Withdrawn - Pregnancy Clinical Trials

The Benefits of Intracytoplasmic Morphologically Selected Sperm Injection (IMSI) in Couples With Unexplained Infertility

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

The (motile sperm organelle morphology examination) MSOME allows the detection of sperm vacuoles that seems to be related to sperm DNA damage. The investigators hypothesized that couples with unexplained infertility could benefit from the injection of spermatozoa selected under high-magnification (x6600)

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: NCT01723293 Recruiting - Pregnancy Clinical Trials

Fetal Cardiovascular Response to Maternal Exercise During Third Trimester

Start date: March 2010
Phase: N/A
Study type: Interventional

The purpose of this study was to examine the behavior of the fetal heart rate in response to different intensities of acute maternal exercise in training and non-training pregnant women

NCT ID: NCT01723098 Recruiting - Pregnancy Clinical Trials

Effect of Regular Exercise on Maternal Cardiovascular System During Pregnancy

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

The main aim of this study was to analysed the security of a supervised exercise program on maternal cardiovascular system and assess the positive effects of this program on maternal cardiovascular function and structure