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NCT ID: NCT00807274 Withdrawn - Kidney Failure Clinical Trials

Renal Function in Adults With Congenital Heart Disease.

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

Impaired kidney function is associated with a poor outcome in patients with heart failure but it is not known of this is the case for patients who have been born with their heart condition (congenital heart disease). This study aims to investigate how frequently patients with congenital heart disease have kidney disease and whither this does have an impact on their outcome. The hypothesis is that kidney dysfunction will be common in these patients and may have an impact on long-term health and life-expectancy.

NCT ID: NCT00789100 Withdrawn - Clinical trials for Chronic Obstructive Pulmonary Disease

Evaluation of Remote Patient Monitoring.

Start date: February 2009
Phase: N/A
Study type: Observational

Nottingham Primary Care Trust has launched telemonitoring to support: independent living and self-management ability of people with congestive heart failure (CHF), chronic obstructive pulmonary disease (COPD) and co-morbidities; and reduce the health care utilisation associated with these patients, including the number of hospitalisations, GP visits and community matron and specialist community nurse home visits. The Multidisciplinary Assessment of Technology Centre for Healthcare (MATCH) will evaluate the technology and its impact of this telemonitoring system on quality of care (i.e. process measures), patient outcomes and direct healthcare costs from an NHS perspective.

NCT ID: NCT00778947 Withdrawn - Clinical trials for Breast Reconstruction

Single Centre Study to Compare Harmonic Scalpel to Conventional Diathermy in Free Tissue Transfer Breast Reconstruction

HARMONIC001
Start date: November 2008
Phase: N/A
Study type: Interventional

The purpose of this single centre study is to evaluate whether the use of Harmonic Synergy Dissecting Hook (Harmonic Scalpel) in breast reconstruction surgery is superior to conventional diathermy in terms of improving ease and speed of perforator dissection, reducing postoperative pain, days of hospital stay and time taken to return to daily activities.

NCT ID: NCT00733759 Withdrawn - Clinical trials for Pulmonary Arteriovenous Malformations

Contrast Echocardiography in Patients With Pulmonary Arteriovenous Malformations (PAVMs)

Start date: February 2004
Phase:
Study type: Observational

Pulmonary arteriovenous malformations (PAVMs) are thin-walled abnormal vessels which provide direct capillary-free communications between the pulmonary and systemic circulations. Patients with PAVMs have usually have low blood oxygen levels and are at risk of other complications including strokes, brain abscesses, pregnancy-related complications and haemorrhage. We hypothesise that the complications of PAVM patients arise from their PAVMs and not the more recognised intracardiac forms of shunting. We propose to perform echocardiograms to enable assessment of the presence of other causes of capillary-free communications between the pulmonary and systemic circulations.

NCT ID: NCT00733629 Withdrawn - Clinical trials for Telangiectasia, Hereditary Hemorrhagic

Study of Endothelial Cells in Patients With Hereditary Haemorrhagic Telangiectasia

Start date: August 2002
Phase:
Study type: Observational

Hereditary Haemorrhagic Telangiectasia (HHT, also known as Osler-Weber-Rendu Syndrome) is an disease that leads to the development of dilated and fragile blood vessels. We propose to culture endothelial cells from patients with HHT, to culture cells that express the proteins mutated in HHT, namely endoglin and ALK-1. We will study the properties of these cells which will involve their growth in different conditions and anticipate that DNA, mRNA and proteins will be extracted from these cells for study of cell responses and association with expression levels of endoglin and ALK-1. We hypothesize that these cells which express "half-normal" endoglin or ALK-1 will show altered protein synthetic differences when compared to normal white blood cells. We anticipate that that these findings may help to explain aspects of the HHT disease phenotype.

NCT ID: NCT00716677 Withdrawn - Asthma Clinical Trials

Dysfunctional Breathing in Difficult Asthma.

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

We plan to use the Life Shirt to record tidal volume, respiratory rate and breathing pattern over a 6 hour period in patients admitted with difficult asthma. The Life Shirt will also be used to collect the same data over the same time period in a group of healthy controls. This data will then be correlated with the assessment of the supervising consultant as to whether the patient has any element of dysfunctional breathing contributing to their symptoms. It is hoped that the data obtained may in future be used to offer treatment to those patients with dysfunctional breathing.

NCT ID: NCT00710827 Withdrawn - Hypogonadism Clinical Trials

Nebido Versus Placebo in Elderly Men With Typical Symptoms of Late Onset Hypogonadism Over a Period of 54 Weeks

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

To evaluate the safety and efficacy of Nebido compared to placebo in elderly men aged 50 and over with symptomatic late onset hypogonadism

NCT ID: NCT00672763 Withdrawn - Crohn's Disease Clinical Trials

Adjuvant Vitamin D With Corticosteroids in Active Crohn's Disease

IBDVit1
Start date: May 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether the addition of vitamin D to standard corticosteroids improves onset of remission in active Crohn's Disease, a form of Inflammatory Bowel Disease (IBD).

NCT ID: NCT00670696 Withdrawn - Healthy Clinical Trials

A Study to Compare the Efficacy of Rapydan Versus Tetracaine Gel

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

Tetracaine gel 4% is a topical anaesthetic gel commonly used in the UK that contains 40 mg of tetracaine base per gram. Adequate anaesthesia can usually be achieved following a 30 minute application time for venopuncture and a 45 minute application time for venous cannulation. The hypothesis is that Rapydan medicated plaster is more effective than tetracaine gel in preventing venous cannulation related pain when applied for the recommended treatment durations of 30 minutes and 45 minutes respectively.

NCT ID: NCT00661973 Withdrawn - Asthma Clinical Trials

Inhaled Corticosteroids on Airway Smooth Muscle in Asthma

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

The main objective is to evaluate how treatment with inhaled corticosteroids (ICS) affects the characteristics of airway smooth muscle (ASM) cells from asthmatic subjects. Our hypothesis is that airway smooth muscle cell dysfunction plays an important role in the pathogenesis of asthma, and that treatment with inhaled corticosteroids reverses the abnormalities in airway smooth muscle cell function.