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Congenital Abnormalities clinical trials

View clinical trials related to Congenital Abnormalities.

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NCT ID: NCT01041469 Completed - Clinical trials for Down Syndrome With and Without Auto Immune Abnormalities

Pilot Study of Auto-immune Abnormalities Associated With Down Syndrome

IMMUTRI
Start date: November 2009
Phase: N/A
Study type: Observational

The purpose of the study is to identify biological data linked to auto immune abnormalities associated with Down Syndrome.

NCT ID: NCT01016756 Completed - PHACE Syndrome Clinical Trials

Genetic Analysis of PHACE Syndrome (Hemangioma With Other Congenital Anomalies)

PHACE
Start date: February 2007
Phase:
Study type: Observational

1. PHACE syndrome(OMIM database number 606519) is the association of a vascular birthmark (hemangioma) on the face along with one or more of the following conditions: congenital heart defects, congenital anomalies of the cerebral arteries,brain, eyes, or sternum. 2. A research study is currently being conducted at the Medical College of Wisconsin (MCW) to investigate if there is an inherited cause of PHACE syndrome. 3. We are hoping that this study will lead to a better understanding of how and why children develop PHACE syndrome.

NCT ID: NCT01007357 Terminated - Clinical trials for Diffuse and Focal Abnormalities of the Liver and Pancreas

Abdominal MR Imaging at 3.0T: Sequence Optimization and Implementation

Start date: December 15, 2009
Phase: N/A
Study type: Interventional

This project will facilitate the optimization of body MR imaging at 3 Tesla.

NCT ID: NCT00990483 Completed - Breast Cancer Clinical Trials

A Comparison of the 15 and 30 Acquisition Angle Breast Tomosynthesis Mammography for Breast Abnormalities

Start date: October 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to conduct an initial investigation into whether an alternative method of using 3D imaging might offer accurate diagnostic performance at a reduced patient radiation exposure in comparison to conventional 2D screening and diagnostic mammography and conventional 2D + 3D imaging methods.

NCT ID: NCT00975819 Active, not recruiting - Clinical trials for Microcystic Lymphatic Malformation

Safety and Efficacy Study of Sirolimus in Complicated Vascular Anomalies

Start date: October 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if the use of sirolimus in the treatment of children and young adults with complicated vascular anomalies will prove to be safe and provide objective response resulting in improved clinical status and quality of life. Funding Source - FDA OOPD (Food and Drug Administration - Office of Orphan Products Development)

NCT ID: NCT00972790 Completed - Epilepsy Clinical Trials

Scalp Nerve Blocks for Post-Craniotomy Pain

Start date: March 2010
Phase: N/A
Study type: Interventional

The objective of this study is to demonstrate that scalp nerve blocks ("scalp freezing"), performed at the end of supratentorial brain surgery, will reduce post-operative pain, opioids side effects, and the time required for post-anaesthesia care unit (PACU)/Intensive Care Unit (ICU) and hospital discharge.

NCT ID: NCT00968565 Completed - Clinical trials for Respiratory Insufficiency

Study Using Citrate to Replace Heparin in Babies Requiring Extracorporeal Membrane Oxygenation (ECMO)

Start date: January 2010
Phase: Phase 0
Study type: Interventional

The purpose of this study is to determine the safety and efficacy of citrate to provide anticoagulation of an ECMO circuit without patient anticoagulation. The standard method of providing ECMO circuit anticoagulation is the use of heparin which also anticoagulates the patient and increases the risk of patient bleeding.

NCT ID: NCT00966537 Recruiting - Pregnancy Clinical Trials

The 3-Dimensional Ultrasound for Fetal Anomaly Scan

Start date: May 2008
Phase: N/A
Study type: Observational

The aim of this study is 1) to study the clinical application of 3D/4D ultrasound for fetal scanning during pregnancy; 2) ) to study the clinical application of 3D/4D ultrasound for pelvic scanning; 3) to demonstrate how to optimally display the different organs. 4) to correlate our findings with other diagnostic tools like MRI, CT; 5) to correlate our findings with clinical outcome.

NCT ID: NCT00964496 Completed - Clinical trials for Obscure Gastrointestinal Bleeding

Long-term Effects of Thalidomide for Recurrent Gastrointestinal Bleeding Due to Vascular Malformation

Start date: November 2004
Phase: Phase 2
Study type: Interventional

Background: Repeated episodes of bleeding from gastrointestinal vascular malformations refractory to endoscopic or surgical therapy often pose a major therapeutic challenge. Methods: The investigators performed a randomized, parallel controlled study of thalidomide as a therapy for recurrent gastrointestinal bleeding due to vascular malformation. Patients with at least six episodes of bleeding in the prior year due to vascular malformation were randomly grouped, prescribed a four-month regimen of either 25 mg of thalidomide or 100 mg of iron orally four times daily, and monitored for at least one year. The primary end point was defined as the patients whose rebleeds decreased from baseline by ≥ 50% at 12 months and the cessation of bleeding. Rebleeding was defined based on a positive fecal occult blood test (FOBT) (monoclonal colloidal gold color technology) at any visit after treatment. Secondary outcomes included the participants dependent on blood transfusions and changes from baseline in transfused packed red cell units, bleeding episodes, bleeding durations, and hemoglobin levels at 12 months. Statistical significance was defined at P < 0.05.

NCT ID: NCT00955370 Completed - Clinical trials for Multiple Abnormalities

The Experience of Uncertainty in Parents of Children With an Undiagnosed Medical Condition

Start date: August 4, 2009
Phase: N/A
Study type: Observational

Background: - Rare and undiagnosed conditions are often chronic and disabling, with symptoms affecting different organ systems at various levels of severity. Perhaps the most challenging feature of an undiagnosed medical condition that has lasted 2 or more years is its characteristic uncertainty. In the absence of a diagnosis, health care professionals can provide only limited treatment and prognostic information. - In the case of a child with an undiagnosed condition, the uncertainty that accompanies what is often a chronic, debilitating medical condition and an undefined prognosis may have physical, psychological, social, and spiritual implications for the entire family. Research suggests that parents of a child with an undiagnosed medical condition may be at significantly increased risk of anxiety, depression, poor health, and overall lower quality of life. - It is not well understood how individuals cope with and adapt to chronic uncertainty, and the factors that influence this process. To design future interventions, descriptive studies are needed to reveal predictors that can be manipulated to improve outcomes. Objectives: - To examine whether perceptions of uncertainty, and perceived personal control, are associated with coping and adaptation. - To examine how the length of time elapsed since child was identified as sick and perceptions of uncertainty affect coping and adaptation. - To assess how perceptions of uncertainty, time elapsed since child became sick, optimism, and perceived personal control affect coping and adaptation. Eligibility: - Parents (older than 18 years of age) of children who have an undiagnosed medical condition. - Participants must have a working e-mail address or fixed postal address. Design: - Parents will be recruited from Web-based support networks for parents of undiagnosed children through Web site postings, electronic mailing lists, and printed newsletter postings. - Participants will be asked to complete a questionnaire about their experiences in living with a child who has an undiagnosed but chronic medical condition. The main outcome variable is adaptation to living with one's child's undiagnosed medical condition. - Participants have the option to complete an online or paper version of the questionnaire. The questionnaire should take between 20 and 30 minutes to complete. - No medical treatments are specifically offered as a part of this study.