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NCT ID: NCT00599534 Withdrawn - Sleep Apnea Clinical Trials

Controlled Trial on Effect of Montelukast Treatment in Children With Obstructive Sleep Apnea Syndrome

Start date: December 2007
Phase: Phase 2
Study type: Interventional

Oral therapy with montelukast may lead to improved polysomnographic findings in children with mild to moderate OSAS with and without allergic rhinitis who a priori require T&A for OSAS. - A significant proportion of the children with OSAS treated with montelukast will show reduced severity of OSAS, and this will obviate the need for surgical T&A.

NCT ID: NCT00598754 Withdrawn - Clinical trials for Aortic Valve Stenosis

Diagnostic Three Dimensional Echocardiography Study Protocol

Start date: June 2001
Phase: N/A
Study type: Observational

The purpose of this study is to perform ground-based research to study what happens to the heart muscle in space. People who have problems with their aortic valve have an increase in the amount of muscle in the left ventricle of the heart. After valve surgery, the amount of muscle should decrease and return to normal. Astronauts lose heart muscle mass during space flight. Our study will look at these changes in your heart, which we believe are similar to what happens during long term space travel. This study will look at the accuracy of three dimensional ultrasound imaging (echo) in monitoring the changes in heart size and function following aortic valve replacement. We are studying ways to prevent health-related problems that men and women will face on long-duration space missions. The hypothesis is that serial two dimensional and three dimensional echo will show accurate changes in the left ventricle mass and volume following aortic valve replacement for aortic stenosis or regurgitation

NCT ID: NCT00598429 Withdrawn - Clinical trials for Pulmonary Hypertension

Inhaled PGE1 in Neonatal Hypoxemic Respiratory Failure

IPGE1
Start date: May 2008
Phase: Phase 2
Study type: Interventional

This pilot study was a randomized, placebo-controlled, clinical trial to test the safety of using the intravenous form of Prostaglandin E1 (PGE1) in an inhaled form for treatment of hypoxemic respiratory failure in term newborns. The study planned to enroll 50 infants diagnosed with hypoxemic respiratory failure at nine NICHD Neonatal Research Network sites, and randomly assign them to receive one dose over a 72-hour period of either high concentration PGE1 (300 ng/kg/min), low concentration PGE1 (150 ng/kg/min), or placebo (normal saline, the diluent for the drug). In addition to determining the safety, optimal dose, and duration of the therapy, this pilot trial planned to evaluate the feasibility of conducting a larger, multi-center randomized, blinded placebo-controlled trial.

NCT ID: NCT00596973 Withdrawn - Diabetes Clinical Trials

Surgical Treatment of Type 2 Diabetes in Non-Morbidly Obese Patients

Start date: January 2008
Phase: Phase 4
Study type: Interventional

The aim of this study is to assess the short term success and feasibility of ileal transposition with sleeve gastrectomy in non-morbidly obese patients with poorly controlled Type 2 Diabetes Mellitus

NCT ID: NCT00594555 Withdrawn - Clinical trials for Acute Myeloid Leukemia

A Study Evaluating the Effects of CLAG With Gleevec in Refractory or Relapsed Acute Myeloid Leukemia

Start date: November 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety of combined chemotherapy treatment (CLAG regimen) with Imatinib Mesylate (Gleevec) in patients with AML.

NCT ID: NCT00594334 Withdrawn - Periodontal Disease Clinical Trials

Effect of Actonel on Periodontal Health of Postmenopausal Women

Start date: January 2008
Phase: Phase 4
Study type: Interventional

Hypothesis: Women who use Actonel (risedronate) for osteopenia will show beneficial periodontal effects.

NCT ID: NCT00594321 Withdrawn - Spinal Fractures Clinical Trials

Evaluation of Fracture Fixation With Energy and Cement in Tumors of the Spine

EFFECTS
Start date: July 2007
Phase: N/A
Study type: Interventional

The objective of the clinical trial is to evaluate the SPACE 360 Delivery System using SPACE CpsXL Bone Cement compared to standard vertebroplasty in the treatment of pathological fractures of the spine caused by metastatic tumors of the spine, myeloma, or lymphoma. Up to a total of three levels per patient may be included or five levels for multiple myeloma. The control group will be standard vertebroplasty.

NCT ID: NCT00594139 Withdrawn - Overactive Bladder Clinical Trials

Autologous Neo-Bladder Construct in Non-Neurogenic Overactive Bladder and Urge Predominant Incontinence

Start date: January 2008
Phase: Phase 2
Study type: Interventional

Subjects with non-neurogenic over-active bladder will be enrolled. The hypothesis is that augmentation cystoplasty using an autologous neo-bladder construct will increase functional capacity and thereby reduce the number of micturition episodes per day in subjects with non-neurogenic over active bladder and urge predominant incontinence.

NCT ID: NCT00593905 Withdrawn - Clinical trials for Pulmonary Hypertension

Pharmacogenomics in Pulmonary Arterial Hypertension

Start date: July 2005
Phase:
Study type: Observational

Our goal is to determine clinically in Pulmonary Arterial Hypertension patients if associations exist between the efficacy and toxicity of sitaxsentan, bosentan, and ambrisentan and several gene polymorphisms in several key disease-specific and therapy specific genes. Also characterized is the relationship between these polymorphisms and the severity of Pulmonary Arterial Hypertension using either baseline hemodynamic or clinical surrogates for disease severity. Hypothesis: Polymorphisms influence the efficacy and toxicity of specific Pulmonary Arterial Hypertension therapy as well as development/severity of PAH via their effect on PA remodeling, drug response, or metabolism. This study requires a one time 8.5 ml blood sample and clinical data to be obtained at initiation of therapy, 4 months after initiation of therapy and 12 months after initiation of therapy.

NCT ID: NCT00593021 Withdrawn - Clinical trials for Obscure Gastrointestinal Bleeding

Diagnostic Evaluation of Obscure Gastrointestinal Bleeding

Start date: October 2007
Phase: N/A
Study type: Observational

Up to 5% of patients with recurrent gastrointestinal (GI) bleeding remain undiagnosed by EGD and colonoscopy, the presumed source of bleeding in these patients being the small intestine. These patients fall under the category of "obscure gastrointestinal bleeding," and frequently require an extensive diagnostic work-up. For these reasons, most patients who present with obscure or occult gastrointestinal bleeding typically undergo multiple endoscopic evaluations, including capsule endoscopy and various radiologic imaging studies, including enteroclysis, small bowel series, CT scan, angiography, and radionuclide scan. Recently, many centers (included the Brigham and Women's Hospital) have begun using capsule endoscopy and CT enterography (CTE) for evaluation of suspected small bowel pathology. This is an observational study enrolling patients referred to the Brigham and Women's Hospital for obscure gastrointestinal bleeding designed to compare the diagnostic yield of various diagnostic modalities, in particular capsule endoscopy and CT enterography in the evaluation of obscure gastrointestinal bleeding.