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Pregnancy Related clinical trials

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NCT ID: NCT03436888 Completed - Pregnancy Related Clinical Trials

Cross-cultural Adaptation and Validation of the Pelvic Girdle Questionnaire in French Language

PELVIC
Start date: March 15, 2018
Phase:
Study type: Observational

The objective of this study is the adaptation of the Pelvic Girdle Questionnaire to the French language from France, and the analysis of its psychometric properties. Firstly, a translation and adaptation process will be performed according to international guidelines. Secondly, the validation process will be performed through a sample of 250 pregnant or postpartum women suffering from pelvic girdle pain. They will fill several questionnaires, including Pelvic Girdle Questionnaire, that will allow us to analyse psychometric properties of the French version.

NCT ID: NCT03433612 Completed - Pregnancy Related Clinical Trials

Improving Accuracy of Landmarks for Neuraxial Blocks in Pregnancy: The Sacral Anatomical Interspace Landmark (SAIL) Technique

SAIL
Start date: February 15, 2018
Phase: N/A
Study type: Interventional

This study is a randomized clinical trial to evaluate the accuracy of the novel SAIL technique compared to the classic intercristal line technique in estimating the L4-L5 interspace for labor epidural or spinal anesthesia placement. The investigators hypothesize that the SAIL technique will be more accurate in successfully locating the L4-L5 interspace in pregnant women than the classic intercristal line technique.

NCT ID: NCT03425916 Completed - Pregnancy Related Clinical Trials

Changes in Abdominal Muscles Performance in Postpartum Women.

Start date: September 1, 2017
Phase:
Study type: Observational

To describe and compare abdominal muscles and inter-rectus distance conditions in postpartum period in comparison with nulliparous women. Also to describe the activation changes during different abdominal exercises.

NCT ID: NCT03422406 Completed - Pregnancy Related Clinical Trials

Research on Excessive Iodine Status in Pregnancy

Start date: January 2016
Phase: N/A
Study type: Observational

To explore main cause and health impact of iodine excess during pregnancy, we performed iodine evaluation for 390 consecutive pregnant women from January 1st, 2016 to December 31st, 2016. Among them, 18 women (4.62%) with apparently elevated urinary iodine concentration (UIC) were enrolled onto this study for subsequent follow-up. History of high iodine exposure was collected from all participants. Parameters about iodine status were monitors until termination of pregnancy, and dietary iodine intake condition and thyroid function were also evaluated.

NCT ID: NCT03419364 Completed - Pregnancy Related Clinical Trials

Study of Nicotinamide in Early Onset Preeclampsia

Start date: November 1, 2017
Phase: Phase 2
Study type: Interventional

Phase II Study of 2.5 gm of nicotinamide, given daily in 3 divided doses, to measure effect on maternal blood pressure in women with early onset preeclampsia and to determine peak and trough levels of nicotinamide. We will compare peak and trough levels in healthy non-pregnant and healthy pregnant participants.

NCT ID: NCT03411993 Completed - Pregnancy Related Clinical Trials

Prevalence of Rheumatic Heart Disease Among Pregnant Women in Kenya

Start date: January 31, 2018
Phase:
Study type: Observational

There is currently no routine screening for cardiac disease for pregnant women in areas of high prevalence. This study will aim to determine the point prevalence of cardiac disease in women presenting for antenatal care at Moi Teaching and Referral Hospital. More specifically, it will aim to use focused echocardiography as a screening tool to determine the prevalence of cardiac disease among pregnant women attending MTRH antenatal clinic.

NCT ID: NCT03410225 Completed - Pregnancy Related Clinical Trials

Motivational Interviewing for Getting Healthy TodaY Study

MIGHTY
Start date: June 1, 2019
Phase: N/A
Study type: Interventional

The present study aims to test and rigorously evaluate the effectiveness of a computer-assisted motivational interviewing (CAMI) intervention that has already been shown to be successful with young women by reducing the risk of rapid subsequent birth among adolescent mothers, and applying this intervention to young men. The purpose of the intervention is to increase condom use, increase female partner use of moderately or highly effective contraception, and increase completion of a reproductive health visit and STI/HIV testing. The primary hypothesis is that the CAMI-TPP (CAMI aimed at Teen Pregnancy Prevention) intervention will increase the proportion of participants who do not engage in risky sex, report condom use at last intercourse as well as partner use of contraception compared to those in the Fitness group. It is also predicted that young men who receive the CAMI-TPP will report higher completion of a reproductive health service visit with sexually transmitted infection (STI) testing over the course of study participation compared to those in the CAMI-Fitness (CAMI aimed at healthy diet, physical activity and tobacco avoidance) group.

NCT ID: NCT03409939 Completed - Pregnancy Related Clinical Trials

Determining Total Aromatic Amino Acid Requirements in Pregnant Women

Start date: February 1, 2018
Phase: N/A
Study type: Interventional

Phenylalanine and tyrosine are aromatic amino acids that people need to obtain in their diets. Amino acids are the building blocks for protein, are are therefore required to form tissues in the body. It is well known that pregnant women require more protein in their diets, but the exact amount for each amino acid is undetermined. To find out how much of phenylalanine and tyrosine pregnant women require, the investigators plan to study pregnant women in early and late gestation with a modern minimally invasive technique.

NCT ID: NCT03408275 Completed - Pregnancy Related Clinical Trials

Dietry Pattern and Lead Levels in Pregnancy

Start date: April 1, 1991
Phase: N/A
Study type: Observational

During pregnancy lead crosses the placenta freely and can have adverse effects on the fetus, with the potential for life-long impact on the child. Identification of dietary patterns and food groups in pregnancy in relation to measures of lead status could provide a more useful alternative to a nutrient-specific advice to minimise fetal exposure to lead during pregnancy. The aim is to evaluate whether dietary patterns and food groups are associated with blood lead concentrations in pregnancy.

NCT ID: NCT03390023 Completed - Pregnancy Related Clinical Trials

Finding Opportunities for Clinical Care and Trial Participation Among Underrepresented Samples

ADORE FOCUS
Start date: March 14, 2018
Phase:
Study type: Observational

Focus groups for Hispanic women who are pregnant and their close family members to assess attitudes, barriers and cultural beliefs involved in participation in clinical trials