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NCT ID: NCT00163813 Not yet recruiting - Critical Illness Clinical Trials

The Early Nasojejunal Tube to Meet Energy Requirements in Intensive Care (ENTERIC) Study

ENTERIC
Start date: n/a
Phase: N/A
Study type: Interventional

This is a multi-centre randomised controlled trial comparing early jejunal feeding (using a frictional nasojejunal [NJ] tube) and standard feeding in critical illness.

NCT ID: NCT00163787 Completed - Amputation Clinical Trials

Clinical Identification of Fall Risk Early After Unilateral Transtibial Amputation

Start date: June 2003
Phase: N/A
Study type: Observational

All participants attend for two testing sessions at either Royal Talbot Rehabilitation Centre or the centre where they received inpatient physiotherapy services. All participants will be tested at discharge and at six months post discharge. Personnel used to score and administer the balance tests at six months will be blinded to pre-test scores, subject background, as well as, mobility and fall history in the six months post discharge. At discharge participants will perform two successful Four Square Step Tests (FSST, and will be videotaped performing the Timed Up and Go Test (TUGT. The turn measure will be scored from this TUGT. Participants will also complete the Locomotor Capabilities index (LCI). At the six-month test participants repeat balance and mobility tests and LCI, as well as being interviewed to ascertain fall history since discharge.

NCT ID: NCT00163774 Completed - Clinical trials for Traumatic Brain Injury

Intensive Monitoring of Brain Injured Patients

Start date: November 2002
Phase: N/A
Study type: Interventional

Analysis of cerebral blood flow (CBF) and oxygenation using complementary focal and global monitoring techniques will permit the delivery of more informed individualised and 'targeted' therapy on the patient with severe head injury, reduce episodes of secondary brain injury and therefore improve outcomes. Aims - To develop a deeper understanding of Cerebral Blood Flow and auto-regulation for TBI patients based on the results of data collected in patients post TBI. - To establish the basis for further multi modality clinical trials in severely brain injured patients in the future. - To improve understanding of the various secondary processes that continue to cause neuronal damage after the initial injury, and therefore affect patient outcome. - To proceed to the second phase of the study, with the introduction of algorithms for treatment.

NCT ID: NCT00163761 Completed - Clinical trials for Non-Hodgkin's Lymphoma

Efficacy Study of Outpatient Therapy for Lymphoma

Start date: December 2002
Phase: Phase 2
Study type: Interventional

This is a Phase II trial evaluating the efficacy (overall response rate) of a risk-adjusted outpatient based approach to lymphoma salvage therapy with vinorelbine, gemcitabine and pegfilgrastim and/or gemcitabine, ifosfamide, vinorelbine and pegfilgrastim.

NCT ID: NCT00163748 Completed - Clinical trials for Non-Hodgkin's Lymphoma

Efficacy and Treatment Related Toxicity Study of a New Regimen for Lymphoma

Start date: February 2001
Phase: Phase 2
Study type: Interventional

This is an open label pilot study of 40 evaluable patients receiving vinorelbine-gemcitabine combination chemotherapy with filgrastim support in an outpatient setting. Participating patients at the time of registration will have measurable relapsed or primary refractory lymphoma.

NCT ID: NCT00163735 Completed - Food Allergy Clinical Trials

Potential Allergens in Wine: Double-blind Placebo-controlled Trial

Start date: August 2002
Phase: N/A
Study type: Interventional

This study is designed to identify whether wines which are produced using the common potential food allergens such as proteins derived from fish, milk or egg are likely to contain sufficient food allergens to cause allergic reactions in susceptible individuals.

NCT ID: NCT00163722 Completed - Clinical trials for Invasive Aspergillosis

A Multicentre Randomised Controlled Trial Comparing Two Strategies for the Diagnosis of Invasive Aspergillosis in High-risk Haematology Patients

Start date: September 2005
Phase: Phase 3
Study type: Interventional

Aspergillus is a fungus found in soil, on farms and on construction sites. In those whose immune system is impaired it causes severe infection. The people who are particularly at high-risk of infection with Aspergillus (which is called Invasive Aspergillosis)are those with acute leukaemia who are having chemotherapy and those post bone marrow transplantation. Currently 15% of those at high-risk develop Invasive Aspergillosis and 60-90% of those with Invasive Aspergillosis die. The main reason for this high death rate is that our current diagnostic tests are not good at detecting infection or often only detect the infection at advanced stages when treatment is ineffective. Because of the limitations of current diagnostic tests the current practice is to give empiric antifungal therapy (EAFT) early to treat suspected Invasive Aspergillosis. However studies have demonstrated that this therapy has only resulted in a minor reduction in the mortality rates and it also causes significant drug toxicity. It is a suboptimal treatment modality. New tests have recently been developed to diagnose Invasive Aspergillosis. These tests are for the detection of an Aspergillus protein in blood and for the detection of Aspergillus DNA in blood. Available data suggests that these new tests make an early diagnosis and seem to be able to monitor responses to treatment. However no study has been reported to date which demonstrates that the use of these tests can impact on important patient outcomes. This trial is being performed to determine whether the use of the new diagnostic tests to guide antifungal therapy will help improve treatment of Invasive Aspergillosis, reduce drug toxicity and reduce the death rate in the high-risk patients as compared with the current standard method of diagnosis and treatment with EAFT.

NCT ID: NCT00163709 Recruiting - Clinical trials for Heart Failure, Congestive

BNP Testing in Patients With SOB on Presentation to ED

Start date: August 2005
Phase: Phase 1
Study type: Interventional

A trial to examine whether a new heart failure blood test can improve the outcome of patients presenting to the Emergency Department with shortness of breath. We hypothesise that a BNP test performed in real-time in patients presenting to the Emergency Department with shortness of breath will help identify additional patients with CHF and consequently to change practice and allow more patients to recieve correct treatment earlier.

NCT ID: NCT00163696 Recruiting - Asthma Clinical Trials

Multi Breath Nitrogen Washout (MBNW) as a Measure of Small Airway Function in Patients With Respiratory Disease

Start date: September 2004
Phase: N/A
Study type: Observational

The researchers are investigating a novel technique, the multi breath nitrogen washout technique, to measure airway changes in various respiratory diseases.

NCT ID: NCT00163683 Completed - Type 2 Diabetes Clinical Trials

Effects of a Mediterranean Style Diet on Vascular Health in Type 2 Diabetes

Start date: January 2003
Phase: N/A
Study type: Interventional

In this study we will compare the effects of a Mediterranean diet, high in fruit and vegetables with the more conventional diet recommended for diabetes therapy (a high carbohydrate, low fat diet) on glycaemic and lipid control and on markers of inflammation, in people with newly diagnosed Type 2 diabetes. The hypothesis is that, over a six-month intervention period, a HVM diet will be more effective than a conventional HCLF diet in improving glycaemic and lipid control, and in reducing markers of vascular inflammation in people with Type 2 diabetes.