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Pregnancy clinical trials

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NCT ID: NCT02573597 Terminated - Pregnancy Clinical Trials

PIEB vs CEI for Labor Analgesia: An MLAC Study

Start date: October 2015
Phase: Phase 4
Study type: Interventional

Utilizing a 'minimal local analgesic concentration (MLAC) study' design to first determine the relative potency of Programmed Intermittent Epidural Bolus (PIEB) compared to Continuous Epidural Infusion (CEI) and secondly to determine the mechanism to explain the potential PIEB efficacy advantage.

NCT ID: NCT02564016 Terminated - Pregnancy Clinical Trials

Efficacy of Labor Epidurals for Postpartum Tubal Ligation

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

The goal of this study is to evaluate the effect of continuous postpartum epidural saline infusion on the reactivation of labor epidurals for postpartum tubal ligation surgery following vaginal delivery.

NCT ID: NCT02546193 Terminated - Pregnancy Clinical Trials

Outpatient Foley Catheter Compared to Usual Inpatient Care for Labor Induction

Start date: September 2015
Phase: N/A
Study type: Interventional

Induction of labor, or causing labor to start before it otherwise starts spontaneously, is sometimes necessary as pregnancy progresses to ensure the safety of both mother and infant. Labor induction often begins with cervical ripening, in which various methods are used to prepare the cervix for contractions and labor. Cervical ripening is beneficial and decreases the need for cesarean section; however, it can be a lengthy process. By tradition, pregnant women are admitted to the hospital at the start of this process and remain inpatient until after the baby is born. There is increasing interest in allowing the mother to return to her own home during the very first part of this process. She may be more satisfied in a more comfortable environment with her family. Growing scientific evidence supports use of the Foley catheter as an approach to outpatient cervical ripening. The Foley catheter is a safe, effective method that is already used often in the inpatient setting. It does not cause increased health risks for either mother or baby. Previous research studies have shown that it is just as safe and effective when women return to their own homes with a Foley catheter and that women spend less time in the hospital before delivery. More information is needed before this becomes a standard of care. This research study will allow pregnant women to return home for the first night of their labor induction with a Foley catheter in place. In the morning they will return to the hospital and stay until after delivery. They will be compared to a group of women who remain in the hospital for their entire labor induction. The benefits to going home during labor induction may include increasing maternal satisfaction and optimizing the use of resources in the hospital.

NCT ID: NCT02537145 Terminated - Obesity Clinical Trials

PregnanT Moms Measure - Do-It-Yourself Health Monitoring and Simulation of Health in Pregnant Women

oPTiMuM
Start date: September 2015
Phase:
Study type: Observational

The aim of this pilot study is to determine the feasibility of Do-It-Yourself studies in pregnant women to detect changes in health parameters by assessing compliance and user experiences of participants. Besides, the measured health will be analysed to increase insight in physiological development in pregnant women.

NCT ID: NCT02510534 Terminated - Pregnancy Clinical Trials

Effect of Luteal Progesterone Support on Pregnancy Rates With Combined Clomid/ Gonadotropin & IUI

Start date: July 2015
Phase: Phase 1
Study type: Interventional

To determine the difference in clinical pregnancy rates with and without luteal progesterone support in a young reproductive aged population having undergone ovulation induction with combined clomiphene citrate and gonadotropin protocol with intrauterine insemination.

NCT ID: NCT02509377 Terminated - Pregnancy Clinical Trials

Fetal Myelomeningocele Repair With Maternal BMI Between 35.0 and 40.0

MOMSto40BMI
Start date: July 2015
Phase: N/A
Study type: Interventional

Inclusion and exclusion criteria for fetal repair of MMC was established by the Management of Myelomeningocele Study (MOMS Trial) and these criteria are the standard of care throughout the United States. These criteria state exclusion for hypertension and diabetes which are known co-morbidities for obesity. Investigators plan to expand one exclusion criteria for open fetal repair surgery. Currently, an exclusion factor is a maternal BMI of 35.0 and greater.Investigators will maintain all other inclusion and exclusion criteria (including excluding for hypertension and diabetes) with the exception of expanding the BMI to include mothers with a BMI of 35.0 to 40.0. Co-morbidities of the research group will be compared to the comorbidities of the mothers published in the MOMS trial.

NCT ID: NCT02493062 Terminated - Pregnancy Clinical Trials

Evaluation of Hysterotomy Site After Open Fetal Surgery

Hysterotomy
Start date: June 2013
Phase: N/A
Study type: Interventional

This study is to review how the uterus heals after having open fetal surgery. Open fetal surgery causes a scar perhaps two: one from the open fetal surgery and a second from delivery by cesarean section; rarely, the same area of your uterus was used for both open fetal surgery and delivery. From other studies of surgery performed on a uterus, some of the uterine scars do not heal well. This study's intervention uses sterile saline to spread open the inside of the uterus. The saline is slowly injected into the uterus using a catheter. An ultrasound called a sonohysterogram is performed to take pictures of the uterus, its inside and the walls of the uterus. In this way, the healed areas from the uterine surgery can be seen with ultrasound and evaluated. This is performed at least 6 months after delivery. Primary Outcome: Measure the depth of the scar and location of the scar 6 months or longer after delivery.

NCT ID: NCT02445092 Terminated - Pregnancy Clinical Trials

The Effect of Pre-washing the Insemination Catheter on Pregnancy Outcome

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

The investigators hypothesize that washing the insemination catheter prior to performing the IUI (intrauterine insemination) will improve the pregnancy outcome in IUI cycles when compared to controls (without pre-washing the catheter). Catheter washing is performed routinely before embryo transfer, however it is not done for IUI catheters. Therefore no data is available on applying the technique to IUI catheters prior to insemination.

NCT ID: NCT02430246 Terminated - Pregnancy Clinical Trials

The Association Between the Transfer of Lactobacilli From the Gastrointestinal Tract to the Vagina and the Prevention / Eradication of Abnormal Vaginal Flora in High Risk Pregnancies

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

Pregnant women at high risk for preterm labor from at least 13 weeks of gestation will be tested to detect abnormal vaginal flora (AVF) or its severe form - bacterial vaginosis (BV) by taking vaginal smear. Treatment will be given according to the results.

NCT ID: NCT02409017 Terminated - Diabetes Clinical Trials

A Comparison of Insulin Drip Protocols in Labor: A Randomized Trial

Start date: April 2015
Phase: N/A
Study type: Interventional

To assess which of two commonly utilized insulin drip protocols has better outcomes when used during the labor process.