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Congenital Abnormalities clinical trials

View clinical trials related to Congenital Abnormalities.

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NCT ID: NCT02505464 Recruiting - Pregnancy Clinical Trials

Pregnancies Complicated by Fetal Anomalies

FAR
Start date: May 2015
Phase:
Study type: Observational [Patient Registry]

The focus of this research is to create a repository of ultrasonographic images and their corresponding medical data from pregnant women (the mothers of the fetuses that are imaged), focusing on fetal anomalies. These women will visit the obstetrical clinics at Regional One Health and the Le Bonheur Fetal Center.

NCT ID: NCT02496013 Recruiting - Lymphedema Clinical Trials

Clinical Translation of a Novel Albumin-Binding PET Radiotracer 68Ga-NEB

Start date: January 2014
Phase: Phase 1
Study type: Interventional

This is an open-label whole-body PET/CT study for investigation of radiation dosimetry, plasma pharmacokinetics, biodistribution, safety and diagnostic performance of 68Ga-NEB in healthy volunteers and patients with suspected infection. Changes of routine blood and urine tests and any adverse events will be collected from the volunteers. Adverse events will also be observed in the patients.

NCT ID: NCT02487641 Recruiting - Obesity Clinical Trials

Obese Pregnant Women: Optimizing Fetal Ultrasound

Start date: June 2015
Phase: N/A
Study type: Observational

This study aim to evaluate the quality of fetal ultrasound in obese pregnant women. The hypotheses is that an early ultrasound will improve the quality of the ultrasound in obese.

NCT ID: NCT02399527 Recruiting - Clinical trials for Lymphatic Malformation

Lymphatic Anomalies Registry for the Assessment of Outcome Data

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

Lymphatic anomalies are a rare subset of vascular anomalies that are poorly understood. the understanding of the natural history, long-term outcomes, risk factors for morbidity and mortality, and the relative benefit of medical therapies and procedures is limited.The goal of this project is to better understand these diseases and improve the care of theses rare patients. To do this, the investigators are conducting an observational study of patients with lymphatic anomalies, including an annual follow-up questionnaire to gather prospective data on mortality, morbidity, treatments, and functionality as well as quality of life.

NCT ID: NCT02358382 Recruiting - Clinical trials for Heart Defects, Congenital

The Management of Systemic-Pulmonary Collateral Blood Flow in Cyanotic Children During Cardiopulmonary Bypass - Pilot Study

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

The purpose of the study is to determine whether it is possible to manage the flow of blood through blood vessels using varying levels of carbon dioxide during cardiac surgery, and what effect this has on how well the major organs of the body work.

NCT ID: NCT02348931 Recruiting - Nose Deformity Clinical Trials

Clinical Effect of a Nasal Former in Nasal Deformities

Start date: December 2013
Phase: Phase 3
Study type: Interventional

Investigation of the effect of customized nasal braces in the correction of nasal deformities with and without prior corrective surgery. - Trial with medicinal product

NCT ID: NCT02257229 Recruiting - Clubfoot Deformity Clinical Trials

Prospective Evaluation of Treatment for Clubfoot

Start date: August 2005
Phase:
Study type: Observational

Specific aim: To evaluate the outcome of infants who undergo one of two nonsurgical treatment interventions

NCT ID: NCT02157597 Recruiting - Clinical trials for Heart Defects, Congenital

NIRS Guidance Trail in Children's Heart Surgery

NIRS
Start date: November 2011
Phase: N/A
Study type: Interventional

Heart surgery in young children involves some risks. This study looks at a new type of monitor that may reduce these risks. Near Infrared Reflectance Spectroscopy (NIRS) aims to measure if enough blood reaches vital organs in the body. The investigators goal is to see if this shows problems developing sooner than usual. The investigators do not know at this time if they can improve the blood supply to the vital organs. The investigators main aim is to see which responses work the best. The NIRS monitor is approved by the U.S. Food and Drug Administration (FDA). The investigators will also follow the progress of recovery after surgery in the Cardiac Intensive Care Unit (CICU). This will find out if using the NIRS monitor improves the outcome for children.

NCT ID: NCT02098252 Recruiting - Clinical trials for Arteriovenous Malformations

Treatment of Brain AVMs (TOBAS) Study

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

The objectives of this study and registry are to offer the best management possible for patients with brain arteriovenous malformations (AVMs) (ruptured or unruptured) in terms of long-term outcomes, despite the presence of uncertainty. Management may include interventional therapy (with endovascular procedures, neurosurgery, or radiotherapy, alone or in combination) or conservative management. The trial has been designed to test a) whether medical management or interventional therapy will reduce the risk of death or debilitating stroke (due to hemorrhage or infarction) by an absolute magnitude of about 15% (over 10 years) for unruptured AVMs (from 30% to 15%); and, b) to test if endovascular treatment can improve the safety and efficacy of surgery or radiation therapy by at least 10% (80% to 90%). As for the nested trial on the role of embolization in the treatment of Brain AVMs by other means: the pre-surgical or pre-radiosurgery embolization of cerebral AVMs can decrease the number of treatment failures from 20% to 10%. In addition,embolization of cerebral AVMs can be accomplished with an acceptable risk, defined as permanent disabling neurological complications of 8%.

NCT ID: NCT02042326 Recruiting - Clinical trials for Arteriovenous Malformations

Prospective Evaluation of the Efficacy of Sirolimus (Rapamune®) in the Treatment of Severe Arteriovenous Malformations

MAV-RAPA
Start date: September 12, 2014
Phase: Phase 2
Study type: Interventional

The aim of the study is to evaluate the efficacy and safety of sirolimus (oral form), to decrease the volume and symptoms due to superficial arteriovenous malformations (AVM). Sirolimus has properties that reduce the activity of the immune system (immunosuppressant), to fight against the proliferation of cancer cells (anti- tumor) and also reduce the proliferation of blood vessels (anti -vascular). Sirolimus is primarily used in transplant patients to prevent organ transplant rejection. Many animal and laboratory studies were carried out and demonstrate in particular the activity of sirolimus on vessels. It is this anti- vascular effect that could help treat arteriovenous malformations.