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Pregnancy clinical trials

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NCT ID: NCT01974531 Completed - Pregnancy Clinical Trials

Psychological Distress & Stress in Parents With Preterm infants-a Prospective Study

Start date: January 2013
Phase:
Study type: Observational [Patient Registry]

The purpose of the present prospective study is the analysis of risk and protective factors of perinatal stress and psychological distress of parents with or without a preterm child. Stress is measured biologically by Cortisol levels and psychologically by a questionnaire. Different outcomes of psychological distress (e.g. anxiety, depression, posttraumatic stress disorder, burnout) are measured by various questionnaires. We analyze the influence of different aspects as personality traits, social support, partnership.

NCT ID: NCT01974050 Completed - Pregnancy Clinical Trials

PregText: Feasibility of Monitoring Influenza Vaccine Safety in Pregnant Women Using Text Messaging

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

In this study, the investigators will prospectively assess fever rates and other adverse events in pregnant women after administration of inactivated influenza vaccine (IIV) using text messaging. The investigators hypothesize that women <20 weeks gestational age who receive IIV will be willing to enroll in a text messaging-based vaccine adverse event monitoring program and will use it to report fever in the post-vaccination period as well as continue to text pregnancy-related outcomes through the end of their pregnancy.

NCT ID: NCT01970436 Completed - Pregnancy Clinical Trials

Personalized Prenatal Care for Low-Risk Pregnancies Using Telemedicine

Start date: May 2014
Phase: N/A
Study type: Interventional

Not all pregnant women have the same risks for pregnancy complications. Women at low-risk for pregnancy complications may not need the same type of prenatal care. The goal of this study is to learn about the use of telemedicine for low-risk pregnant women and improve the delivery of prenatal care. Telemedicine is medical care provided using a computer or telephone to visit with a doctor for some medical appointments. Participating patients will be assigned by a computer to either standard prenatal care, or prenatal care involving a combination of standard prenatal visits and telemedicine visits. Both groups will have the same number of prenatal care visits. In both groups, we will ask about the patients' satisfaction with their care, the amount of time they spent visiting with their doctor, and information about time and their expenses. In the telemedicine group, we will teach how to measure blood pressure, fetal heart rate, and weight from home. The goals of this study are to: 1) assess the patient satisfaction, patient experiences and preferences, financial impact, clinical outcomes, and provider satisfaction of providing personalized prenatal care for low-risk pregnancies using telecommunication and remote patient care devices; and 2) measure the reliability of at-home, patient-recorded, computer-documented prenatal care measurements. The primary outcome is patient satisfaction with prenatal care after delivery.

NCT ID: NCT01962831 Completed - Obesity Clinical Trials

Randomized Controlled Trial: Induction of Labour of Obese Women With Dinoprostone or Single Balloon Catheter

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

The purpose of this study is to compare the efficacy of single balloon foley catheters to dinoprostone for the induction of labour of obese women. The investigators suspect that women assigned to the foley group will have a shorter induction to delivery time than women in the dinoprostone group.

NCT ID: NCT01962701 Completed - Pregnancy Clinical Trials

Fetal Copeptin After Oxytocin Challenge Test

CopOCT
Start date: January 2013
Phase: N/A
Study type: Observational

The relationship of uterine contractions on fetal copeptin levels in umbilical cord blood is studied.

NCT ID: NCT01959464 Completed - Pregnancy Clinical Trials

Sexual Absorption of Vaginal Progesterone

Start date: November 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if sexual intercourse lowers serum progesterone in women using vaginal progesterone gel (Crinone®), and increases serum progesterone in their male sexual partners. We hypothesize, based on previous estrogen studies done by our group, that intercourse will interfere with absorption of vaginal progesterone.

NCT ID: NCT01958307 Completed - Pregnancy Clinical Trials

Healthy Living in Pregnancy

GeliS
Start date: September 2013
Phase: N/A
Study type: Interventional

Multicenter and multidisciplinary public health project in 10 regions of Bavaria, a federal state of Germany, targeting maternal and fetal health. The objective of this trial is to evaluate the efficacy of a lifestyle intervention program focusing on diet, physical activity and weight monitoring during pregnancy. The intervention comprises 4 individual counseling sessions addressing healthy living. Primary outcome: gestational weight gain. Secondary outcomes are pregnancy and obstetric complications like gestational diabetes and rate of caesarean sections as well as offspring health. The lifestyle intervention program is adapted to the German health care system to allow an immediate implementation after successful evaluation.

NCT ID: NCT01948596 Completed - Depression Clinical Trials

The Synchronized Trial on Expectant Mothers With Depressive Symptoms by Omega-3 PUFAs (SYNCHRO): Open Trial

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

The present study aims to examine the efficacy and safety of omega-3 polyunsaturated fatty acids for pregnant women with depressive symptoms.

NCT ID: NCT01948258 Completed - Pregnancy Clinical Trials

Clearblue Advanced Fertility Monitor Consumer One Cycle at Home Study

Start date: March 1, 2013
Phase: N/A
Study type: Interventional

This study will assess the use of the new Clearblue Advanced Fertility Monitor for one menstrual cycle in a home setting by female volunteers seeking to get pregnant.

NCT ID: NCT01945424 Completed - Pregnancy Clinical Trials

Sanofi Pasteur Quadrivalent Influenza Vaccine (QIV) Pregnancy Registry

Start date: August 16, 2013
Phase:
Study type: Observational [Patient Registry]

The Sanofi Pasteur Quadrivalent Influenza Vaccine (QIV) Pregnancy Registry will be a prospectively recruited pregnancy surveillance program designed to collect and analyze information on vaccine exposures, pregnancy outcomes, and fetal and offspring outcomes.