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Pregnancy clinical trials

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NCT ID: NCT02038023 Completed - Pregnancy Clinical Trials

Intravaneous Iron(1000 mg Low Molecular Weight Iron Dextran Over 60 Minutes) for Pregnant Women

Start date: July 2013
Phase: Phase 2
Study type: Interventional

To determine the percentage of women who achieve anemia correction after a single dose of 1000mg of low molecular weight iron dextran(infed).

NCT ID: NCT02035059 Completed - Pregnancy Clinical Trials

Predictability of Gestational Diabetes Mellitus in First and Second Trimester

GDMPredict
Start date: May 1, 2014
Phase:
Study type: Observational

The objective of the study is, if an early oral glucose tolerance test combined with maternal history, condition and multiple biomarker analysis can be used to detect gestational diabetes mellitus in the first trimester (12-14 weeks of gestation).

NCT ID: NCT02032459 Completed - Pregnancy Clinical Trials

Vitamin D and Pregnancy: Camden Study

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

Vitamin D is present in food either naturally or by fortification and included in nutritional supplements. It is also synthesized photochemically by the skin from ultraviolet B radiation. Vitamin D synthesis varies by season and with latitude as well as according to intensity of skin pigmentation. Recent research in the United States found lower circulating levels of 25 (OH) D, the primary indicator of vitamin D status, among minority women who were either pregnant or in their reproductive years. The extent to which maternal vitamin D has an influence on the course and outcome of human pregnancy remains to be more completely studied. We propose to use the HPLC method to assay cholecaliferol (vitamin D3) and ergocalciferol (vitamin D2) to assess maternal vitamin D status. This will be accomplished by analyzing existing fasting samples and data derived from the 2001-2006 cohort (N=1141) of young, low income minority gravidae from Camden, New Jersey to determine: 1. The prognostic importance of maternal vitamin D status for birth weight, gestation duration and poor pregnancy outcomes (low birth weight, preterm delivery, fetal growth restriction). 2. The relation of maternal vitamin D status to important complications of pregnancy (gestational diabetes and pre-eclampsia). 3. The relationship of maternal vitamin D status to maternal diet and supplement use, season of year, ethnicity, overweight/obesity, and other maternal characteristics.

NCT ID: NCT02029859 Completed - Obesity Clinical Trials

Sleep Apnea, Obesity and Pregnancy

GOS
Start date: April 2011
Phase: N/A
Study type: Interventional

Main objective: Determine the prevalence of obstructive sleep apnea syndrome (OSA) in late pregnancy in a population of obese patients . Secondary objectives : - Identify risk factors for OSA during pregnancy (age, parity, high blood pressure, snoring , weight, neck circumference, scores on symptoms of sleep apnea, ... ) . - Compare perinatal morbidity among obese patients with OSA in late pregnancy with case-controls. - Evaluate the evolution of a moderate or severe OSA 6 months after pregnancy. Material and methods Characteristics of the study: - Interventional biomedical research - Prospective Multicenter nonrandomized study Flow chart - Patients will be included between 30 and 36 weeks of amenorrhea (WA) . - Will rated from inclusion: age, parity, weight, height, BMI in early pregnancy, neck circumferrence, treated high blood pressure. - As recommended in France, the main test results during the pregnancy follow-up will be recorded. - At the inclusion visit will be conducted a Berlin Questionnaire and Epworth Score. - Screening for OSA by nocturnal polysomnography will be performed between 30 and 36WA. This screening can be performed as an outpatient. - In case of proven OSA patients will be offered an appropriate care by today's standards. - Whatever the outcome of pregnancy, a second polysomnography will be performed 6 months after childbirth in case of OSA during pregnancy.

NCT ID: NCT02028000 Terminated - Pregnancy Clinical Trials

Postoperative Pain and Skin Closure Methods After Cesarean Section

Skin
Start date: January 2012
Phase: N/A
Study type: Interventional

The study is looking at women undergoing cesarean section delivery of their baby. The purpose of this research study is to determine what type of skin closure after cesarean section helps decrease pain level the most and improves the appearance of the incision site. The study hypothesis is to determine if skin closure with absorbable subcuticular staples leads to improved cosmesis and/or decreased post-operative pain. Participants in the study will already be scheduled for a cesarean section for delivery of their baby. They will be randomized into one of three groups, 1) Insorb (absorbable subcuticular stapes), 2) Vicryl suture or 3) Monocryl suture for the skin closure of their cesarean section. Information that will be recorded includes amount of pain medication usage while in the hospital after cesarean section, daily patient rated pain score until discharge from hospital, pain score 6 weeks after surgery and cesarean section cosmetic scar 6 weeks after surgery.

NCT ID: NCT02025673 Active, not recruiting - Type 2 Diabetes Clinical Trials

Study of Betatrophin Levels in Patients With Type 2 Diabetes and Gestational Diabetes and Healthy Subjects

Start date: August 2013
Phase: N/A
Study type: Observational

Betatrophin is a newly identified hormone that promotes pancreatic beta cell proliferation, improves glucose tolerance and regulates lipids metabolism. A recent study showed that circulating concentrations of betatrophin doubled in type 1 diabetes. The objective of this study is to investigate the association of serum betatrophin levels with the progression of diabetic retinopathy in patients with type 2 diabetes and the level of betatrophin in gestational diabetes patients and pregnant women.

NCT ID: NCT02024048 Active, not recruiting - Pregnancy Clinical Trials

Evaluation of Choroidal Thickness During Pregnancy Using Enhanced Depth Imaging Optical Coherence Tomography

Start date: December 2013
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to evaluate choroidal thickness and volume during the third trimester of pregnancy by comparison with a group of age-matched non-pregnant healthy group of women

NCT ID: NCT02021799 Completed - Pregnancy Clinical Trials

The Effect of Under-nutrition on the Human Microbiota

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

The purpose of this study is to determine whether a difference exists in the gut, oral, vaginal and human milk microbiome of under-nourished pregnant women as compared to healthy and obese pregnant women. In addition, the investigators are setting out to determine if a micronutrient enriched probiotic yogurt can improve the microbiome and pregnancy outcomes of under-nourished pregnant women.

NCT ID: NCT02018640 Completed - Cancer Clinical Trials

Biomarker Feedback to Motivate Tobacco Cessation in Pregnant ALaska Native Women: Phase 2

MAW Phase 2
Start date: December 2013
Phase: N/A
Study type: Observational

Use of tobacco is very high among Alaska Native pregnant women. The investigators are conducting a three phase study. The first study is nearly completed and involved measuring biomarkers of tobacco exposure in mothers and infants. The second phase of the research is a qualitative study to translate the biomarker findings to an intervention.

NCT ID: NCT02017080 Recruiting - Clinical trials for Hypothyroidism in Pregnancy

Fetal Thyroid Ultrasound And Fetal Thyroid Hormones

Start date: January 2014
Phase: N/A
Study type: Observational

Non invasive methods: maternal antithyroid antibodies and ultrasound measurement of the fetal thyroid gland could be an important tool for detecting fetal thyroid dysfunction in mothers with autoimmune thyroid disease.