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NCT ID: NCT00585403 Withdrawn - Obesity Clinical Trials

Exercise Changes to Peripheral Blood Mononuclear Cells in Children

Start date: December 2004
Phase:
Study type: Observational

The goal of this research is to determine how the peripheral immune system is altered by exercise and differences related to gender, pubertal status and health.

NCT ID: NCT00585234 Withdrawn - Clinical trials for Thoracic Insufficiency Syndrome

Tools for the Objective Clinical Assessment of Pediatric Spinal Deformity

Start date: December 2005
Phase:
Study type: Observational

This project seeks to develop a standardized technique for simultaneous capturing bi-planar images of patients against a standard background with a grid that can be used later for the quantitative determination of global balance and thoracic symmetry. We hypothesize that patients who are successfully managed with surgery will demonstrate an improvement in global balance and thoracic symmetry that can be accurately measured. This measurement station will be specifically developed to provide a standardized, reproducible means to compare clinical assessments of surgical and non-surgical outcomes, and establish normative data for comparison. This standardized tool can be established at multiple centers for use in multicenter trials.

NCT ID: NCT00584675 Withdrawn - Clinical trials for Gastroesophageal Reflux Disease

Nasopharyngeal 24 Hour pH Monitoring in Health Adult Volunteers

Start date: February 2007
Phase: N/A
Study type: Interventional

Involves a 24-hour pH probe study using the Dx-pH Measurement System on patients who do not have symptoms of laryngopharyngeal reflux or gastroesophageal reflux disease to establish normal values for the Dx-pH Measurement System.

NCT ID: NCT00584636 Withdrawn - Asthma Clinical Trials

Pulmicort Respules on Relapse Rates After Treatment in the ED

Budesonide
Start date: October 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to see if the addition of budesonide to oral corticosteroids will result in a decrease in relapse rates compared to oral corticosteroids alone in children who are discharged from the ED after an asthma exacerbation. Secondly, that there will be an improvement in lung function, a decrease in beta-2 agonist use and an improvement in health-related quality of life compared to placebo.

NCT ID: NCT00584623 Withdrawn - Dysphagia Clinical Trials

Simultaneous Fluoroscopic and Endoscopic Examination of the Oropharyngeal Phase of Deglutition

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

To correlate findings between two commonly-used types of swallowing studies: videofluoroscopy and flexible endoscopic evaluation of swallowing (FEES).

NCT ID: NCT00584545 Withdrawn - Dysphagia Clinical Trials

Simultaneous Fluoroscopic and Manometric Measures of the Oropharyngeal Phase of Deglutition

Start date: June 2007
Phase:
Study type: Observational

To validate the pharyngeal constriction ration, a surrogate measure of pharyngeal strength on fluoroscopy by comparing it with simultaneous pharyngeal manometry.

NCT ID: NCT00584337 Withdrawn - Clinical trials for Coronary Artery Disease

Coronary CT Angiography as the Primary Initial Method of Evaluating Patients With Subacute Chest Pain (CT PRIME)

CTPRIME
Start date: January 2008
Phase: N/A
Study type: Observational

This study is designed to evaluate a new approach to the diagnosis of chronic or sub-acute chest pain patients in the out-patient setting. Patients in this study are selected to be "low-risk", meaning they are not having an acute or recent heart attack (AMI), based on screening blood tests and electrocardiograms (EKGs). In addition, these patients have a low or intermediate pre-test likelihood of the coronary artery disease (CAD), which means that probability of the CAD based on the available clinical and historical information, does not make a diagnosis of the CAD a certain clinical diagnosis in the particular patient and this, in turn, requires an additional diagnostic work up.

NCT ID: NCT00584246 Withdrawn - Clinical trials for Restless Legs Syndrome

Pregabalin (Lyrica) for the Treatment of Restless Legs Syndrome

Start date: November 2007
Phase: Phase 4
Study type: Interventional

This study will evaluate the safety and efficacy of Pregabalin (Lyrica) in treating patients with Restless Legs Syndrome (RLS) in a double-blind, placebo-controlled trial.

NCT ID: NCT00584155 Withdrawn - Hearing Loss Clinical Trials

Protection From Cisplatin Ototoxicity by Lactated Ringers

Start date: July 2006
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine if Lactated Ringer's solution is effective in patients undergoing chemotherapy with cisplatin for head and neck cancer in regards to cisplatin-induced hearing loss.

NCT ID: NCT00584090 Withdrawn - Parkinson's Disease Clinical Trials

Solifenacin Succinate (VESIcare) for the Treatment of Urinary Incontinence in Parkinson's Disease

Start date: November 2007
Phase: Phase 4
Study type: Interventional

The primary purpose of this study is to measure the efficacy of solifenacin succinate (VESIcare) on treating urinary incontinence in Parkinson's disease patients. The secondary objective of this study is to examine the effect of solifenacin succinate (VESIcare) on symptoms of PD and the patient's quality of life.