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Pregnancy Related clinical trials

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NCT ID: NCT03769610 Terminated - Pregnancy Related Clinical Trials

Inpatient Versus Outpatient Cervical Ripening

Start date: January 4, 2017
Phase: N/A
Study type: Interventional

Induction of labor is a process of stimulating uterine contractions before the onset of labor, with a goal of achieving vaginal birth. The cervix (the lower part of the uterus that connects to the vagina) must dilate (open) in order to allow passage of the baby into the vagina and through the birth canal. A process called "cervical ripening" is often performed prior to labor induction to prepare the cervix for labor and therefore shorten the length of the labor. There are various pharmacologic and mechanical methods of cervical ripening that result in the physical softening and distensibility of the cervix. Mechanical dilation with a small balloon (i.e. a Foley catheter) placed in the cervix is one of the most commonly used, safe, inexpensive, and effective methods to achieve cervical ripening. In most hospitals, cervical ripening is performed in the hospitals; however, some hospitals allow women to undergo cervical ripening at home with a transcervical Foley catheter. The goal of this study is to compare the use of a Foley catheter for cervical ripening in the inpatient (in-hospital) and outpatient (at home) settings. We anticipate that outpatient use will lead to a shorter amount of time that a woman spends in the hospital, decreased cost, and good patient satisfaction.

NCT ID: NCT03765684 Recruiting - Pregnancy Related Clinical Trials

Factors Affecting Newborn Body Composition and Later Health in Helsinki Birth Cohort 2018-2022

HeBiCo
Start date: December 1, 2018
Phase:
Study type: Observational

In Helsinki Birth Cohort 2018-2022 a large, longitudinal and well-phenotyped birth cohort of infants and their parents will be established. Mothers, fathers/spouses and their children in Helsinki and Uusimaa Hospital District are recruited in the study and newborn composition of the children born in Helsinki Women's Hospital will be measured. Data on maternal and paternal diet quality, physical activity and depression during and after pregnancy will be collected and data from the hospital and national registers will be collected. Health of offspring and parents will be followed during their later life.

NCT ID: NCT03763071 Completed - Pregnancy Clinical Trials

Sleep Disturbances in the 2nd and 3rd Trimester

Start date: December 7, 2018
Phase:
Study type: Observational

Sleep disorders and disturbances are mostly underestimated in clinical practice. Moreover, this problem is generally neglected by the pregnant themselves. Today, it is important to underline any problem that may have an affect to improve the quality of life during pregnancy. This study assesses the sleep quality, insomnia patterns and obstructive sleep apnea in the second and third trimesters of pregnancy.

NCT ID: NCT03762512 Recruiting - Pregnancy Related Clinical Trials

Collection of Placenta for Mitochondria Isolation

Start date: December 1, 2018
Phase:
Study type: Observational

Placenta will be collected and from these, mitochondrial will be harvested. Mitochondria will be used in mitochondrial augmentation therapy.

NCT ID: NCT03750968 Completed - Pregnancy Related Clinical Trials

Lutein & Zeaxanthin in Pregnancy - Carotenoid Supplementation During Pregnancy: Ocular and Systemic Effects

L-ZIP
Start date: September 26, 2019
Phase: Phase 2
Study type: Interventional

This study is designed to test the hypotheses that (1) the third trimester of pregnancy is a period of maternal systemic and ocular carotenoid depletion; (2) prenatal supplementation with 10 milligrams of lutein and 2 milligrams of zeaxanthin will have significant effects on ocular and systemic biomarkers of maternal and infant carotenoid status relative to a matched, standard-of-care prenatal supplement without added lutein and zeaxanthin; and (3) newborn infants with the highest systemic and ocular carotenoid status will have more mature foveal structure. Mothers will be enrolled in the study during their first trimester, and will take the study carotenoid or control supplements for 6 to 8 months. The final study outcome measurements of mothers and infants will be completed within two weeks of the baby's birth.

NCT ID: NCT03748888 Completed - Pregnancy Related Clinical Trials

Physical Exercise Cardiovascular Adaptation Monitoring in Pregnancy (PE-CAMP Study)

PE-CAMP
Start date: April 26, 2018
Phase: N/A
Study type: Interventional

The main theme of this study focuses on providing evidence of the impact of antenatal physical activity on maternal/foetal cardiovascular changes during pregnancy and maternal cardiovascular adaptations during the early postpartum period.

NCT ID: NCT03738267 Recruiting - Clinical trials for Head and Neck Cancer

Study on the Occurrence of Head and Neck Cancers During Pregnancy

REFCORbirth
Start date: November 7, 2018
Phase:
Study type: Observational

Head and neck cancers that occurred during pregnancy

NCT ID: NCT03737279 Completed - Pregnancy Related Clinical Trials

Daily Meditation Program in Women Admitted to the Antepartum Unit

Meditate
Start date: March 4, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to assess whether a daily mindful meditation program for women admitted to the antepartum floor will decrease maternal state anxiety compared to routine care.

NCT ID: NCT03733405 Completed - Pregnancy Related Clinical Trials

Postpartum Care Timing: A Randomized Trial

PUnCTuAL
Start date: October 31, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if shortening the time to initial postpartum visit from six weeks to two weeks can improve clinic visit attendance and decrease usage of the emergency department.

NCT ID: NCT03731871 Recruiting - Pregnancy Related Clinical Trials

Parameters of Lung Maturity During Late Pregnancy

Start date: November 12, 2018
Phase:
Study type: Observational

- Lung maturity is one of the most important factors in perinatal medicine