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NCT ID: NCT03146156 Active, not recruiting - Obesity Clinical Trials

Lifestyle Intervention in Preparation for Pregnancy (LIPP)

Start date: March 21, 2017
Phase: N/A
Study type: Interventional

Studies evaluating lifestyle intervention in obese women during pregnancy have reported limited success in decreasing excessive gestational weight gain, and have failed to achieve the key outcome of breaking the obesity cycle and reducing neonatal adiposity or birth weight. Although some investigators advocate weight loss during pregnancy in obese women, these recommendations were based on extrapolation of retrospective epidemiological data. Of concern, we reported increased small for gestational age babies and decreased lean body mass in neonates of obese women with weight loss or inadequate gestational weight gain. Based on our research, optimal outcomes from lifestyle interventions are likely to be temporal and therefore must be initiated prior to conception to first improve maternal metabolic function, and subsequently, placental/fetal growth. Several large retrospective cohort studies support our hypothesis. For example, women who lost weight between pregnancies had fewer large for gestational age babies in contrast to women who increased interpregnancy weight. In addition, prospective randomized controlled trials have shown that postpartum weight loss is achievable without adverse maternal or neonatal outcomes, these studies include women who breastfed. Based on these observations, we propose a randomized control trial to determine the effect of lifestyle intervention initiated prior to a planned pregnancy on improving neonatal metabolism and adiposity. Our overarching hypothesis is that the maternal pre-pregnancy metabolic condition determines the obesogenic in-utero environment, which affects programming of placental mitochondrial function and metabolic pathways, promoting lipid accumulation and neonatal adiposity. Our rationale is based on the need to establish the most effective time to introduce an intervention that will break the obesity cycle in mothers and their children. Understanding how pregravid metabolic conditioning improves maternal physiology, and cellular and molecular function in pregnancy will provide the empirical data to support the intervention. We have a highly successful record of recruiting women who are planning a pregnancy, obtaining compliance in longitudinal studies, and in long-term follow-up of mothers and their offspring. Lifestyle intervention will be initiated prior to conception to decrease maternal body fat, inflammation, insulin resistance, and ?-cell dysfunction. Our transdisciplinary team has the required expertise in lifestyle interventions management of obesity, and in human physiology that is needed to determine the effects of these interventions on maternal metabolism and fetalplacental growth and function. We will recruit 200 women to pursue the following specific aims: Specific Aim 1: To investigate the physiological significance of lifestyle intervention in preparation for pregnancy (LIPP) on maternal and neonatal metabolism and adiposity. Specific Aim 2: To determine the molecular effects whereby lifestyle intervention initiated before pregnancy can improve placental mitochondrial lipid oxidation and accumulation.

NCT ID: NCT03146078 Active, not recruiting - Clinical trials for Usher Syndrome, Type 2A

Rate of Progression in USH2A-related Retinal Degeneration

RUSH2A
Start date: August 11, 2017
Phase:
Study type: Observational

The overall goal of this project funded by the Foundation Fighting Blindness is to characterize the natural history of disease progression in patients with USH2A related retinal degeneration associated with congenital hearing loss (Usher syndrome type 2a) or non-syndromic retinitis pigmentosa (RP39).

NCT ID: NCT03145636 Active, not recruiting - Obesity, Morbid Clinical Trials

The ReNEW Study: Maestro® New Enrollment Post-Approval Study Protocol

ReNEW
Start date: August 30, 2017
Phase: N/A
Study type: Interventional

This is a five-year, single arm, multi-center trial to evaluate the long-term safety and efficacy of the Maestro Rechargeable System in treating obesity. The study will include an observational arm and a randomized sub-study.

NCT ID: NCT03145532 Active, not recruiting - Cerebral Palsy Clinical Trials

Transcranial Direct-Current Stimulation (tCDS) and Robotics for Children With Hemiplegia

Start date: June 12, 2017
Phase: N/A
Study type: Interventional

Hemiplegia occurs when the function of motor areas in the brain become impaired, predominantly unilaterally, during perinatal development. Children with hemiplegia show impairments in motor control of the affected side of the body. Impairments in use of the upper extremity are common, and lead to functional disability throughout the lifespan of a person with hemiplegia. Upper extremity impairments can severely affect a person's ability to carry out activities of daily living. The goal of this study at Blythedale Children's Hospital is to test the efficacy of transcranial direct current stimulation (tDCS) and robotic upper extremity therapy in improving upper extremity function in children with unilateral cerebral palsy. This study will test the hypothesis that physical rehabilitation, provided by repetitive arm movements guided by a robot, will improve upper extremity function in children with hemiplegia, and that this improvement can be enhanced by transcranial direct current stimulation of motor cortex immediately before robotic training.

NCT ID: NCT03145337 Active, not recruiting - Clinical trials for Breast Reconstruction

Reconstruction Outcomes in Immediate Post-mastectomy Breast Reconstruction With ADM

Start date: July 1, 2017
Phase: N/A
Study type: Interventional

Evaluation and comparison of clinical and aesthetic outcomes associated with the use of two allograft dermal matrices (ADMs) currently in use for tissue assisted immediate post-mastectomy breast reconstruction.

NCT ID: NCT03145142 Active, not recruiting - Premature Birth Clinical Trials

PREMOD2 With Near Infrared Spectroscopy Sub-study

PREMOD2
Start date: June 6, 2017
Phase: N/A
Study type: Interventional

Early hemodynamic effects (within 3 hours of life) of Delayed Cord Clamping compared to Umbilical Cord Milking are still unknown. Four sites experienced in the use of NIRS and who have appropriate data collection equipment in the delivery room (Alberta, Ulm, Cork and San Diego) will obtain and report the physiological changes with UCM and DCC from birth until 24 hours of life. This data will yield the largest available sample of continuously recorded heart rate, cerebral tissue oxygenation, peripheral oxygen saturation, airway pressure, and administered FiO2 to delineate the short term responses to two methods of placental transfusion. In our initial trial we demonstrated increased blood pressure from 3-15 HOL with UCM compared to DCC in premature newborns <32 weeks, but did not show any differences in cerebral oxygenation.

NCT ID: NCT03144765 Active, not recruiting - Surgery Clinical Trials

Multicenter Phase II Study of Transanal TME (taTME)

Start date: January 19, 2018
Phase: N/A
Study type: Interventional

Radical rectal cancer resection, namely total mesorectal excision (TME), is the cornerstone of the treatment of resectable rectal cancer. In combination with chemotherapy and radiation treatment (CRT), complete TME with negative resection margins is associated with sustained local and systemic control even in locally advanced disease. Over the last 2 decades, laparoscopic and robotic techniques have been increasingly adopted due to reduced surgical trauma and faster patient recovery. Yet, both approaches are associated with equivalent postoperative morbidity and disturbances in sexual, urinary and defecatory function relative to open TME. Furthermore, laparoscopic and robotic TME remain associated with substantial conversion rates and variable rates of TME completeness as a result of the procedural difficulties reaching the low rectum from the abdominal approach. Transanal TME (taTME) with laparoscopic assistance was developed to facilitate completion of TME using a primary transanal endoscopic approach. Transanal TME uses a "bottom-up approach" to overcome the technical difficulties of low pelvic dissection using an abdominal approach. Published results from single-center taTME series and an international registry suggest the short-term procedural and oncologic safety of this approach in resectable rectal cancer. No multicenter phase II study has yet been conducted to validate the procedural safety, functional outcomes or long-term oncologic outcomes of this approach. Study Design: This is a 5-year phase II multicenter single-arm study to evaluate the safety and efficacy of low anterior resection (LAR) with taTME using laparoscopic or robotic assistance in 100 eligible subjects with resectable rectal cancer. Hypothesis: taTME is non-inferior to standard LAR with respect to the quality of the TME achieved.

NCT ID: NCT03144674 Active, not recruiting - Lymphoma Clinical Trials

A Study of INCB050465 in Subjects With Relapsed or Refractory Marginal Zone Lymphoma (CITADEL-204)

Start date: December 18, 2017
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of two parsaclisib treatment regimens in participants diagnosed with relapsed or refractory marginal zone lymphoma (MZL) who are naive to or were previously treated with a Bruton's tyrosine kinase (BTK) inhibitor.

NCT ID: NCT03143439 Active, not recruiting - Clinical trials for Responsible Fatherhood Programming

Evaluation of the Fathers Advancing Communities Together (FACT) Program

Start date: July 2016
Phase:
Study type: Observational

The Urban Institute-a nonprofit, nonpartisan research organization-is partnering with Rubicon Programs to conduct a rigorous evaluation of its Fathers Advancing Communities Together (FACT) program. FACT is a multi-faceted program designed to deliver responsible parenting, healthy relationships, and economic stability services on a voluntary basis to low-income fathers in Contra Costa County, California. Urban's evaluation comprised of three key components: The implementation evaluation will describe FACT program activities and services, including communication and coordination across partners, service delivery mechanisms, and whether and how participants and their families received comprehensive services. Urban will identify a logic model for the program and assess the barriers to and facilitators of program performance. The implementation evaluation will draw from interviews with program staff, partners, and stakeholders, as well as field observations, program and administrative data, and focus groups with FACT participants and their families. The outcome evaluation will build on the implementation evaluation to determine whether specific program components, their frequency, and their duration, are related to outcomes. Urban will conduct surveys of program participants at the time of their enrollment into the program and one year following their enrollment to explore how participants' self-reported attitudes on various domains are associated with economic self-sufficiency and family functioning. Urban will also use program and administrative data collected by Rubicon and its partners, specifically Rubicon's case management database, to assess participant outcomes. The impact evaluation will assess to what extent participation in the FACT program is associated with improved outcomes as compared to similarly situated individuals who did not participate in the program. Urban will work with Rubicon's partners to identify individuals living in Contra Costa County who were eligible to participate in the program but, for whatever reason, did not do so. Once a comparison group of fathers has been established, Urban will use individual-level outcome data to determine whether the FACT program has an impact on economic self-sufficiency and family functioning.

NCT ID: NCT03143270 Active, not recruiting - Liver Cancer Clinical Trials

A Study to Test the Safety and Feasibility of Nivolumab With Drug Eluting Bead Transarterial Chemoembolization in Patients With Liver Cancer

Start date: April 28, 2017
Phase: Early Phase 1
Study type: Interventional

The purpose of the study is to find out the effects of using nivolumab with Drug Eluting Bead Transarterial Chemoembolization (deb-TACE) in the treatment of liver cancer.