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NCT ID: NCT02652741 Not yet recruiting - Heart Failure Clinical Trials

Orodispersible Minitablets of Enalapril in Young Children With Heart Failure Due to Congenital Heart Disease

LENA-WP09
Start date: January 2016
Phase: Phase 2/Phase 3
Study type: Interventional

Paediatric clinical trial in 50 children, from newborn to less than 6 years of age, suffering from heart failure due to congenital heart disease, to obtain paediatric pharmacokinetic and pharmacodynamic data of enalapril and its active metabolite enalaprilat while treated for 8 weeks with enalapril in form of Orodispersible Minitablets (ODMTs), to describe the dose exposure in this patient population.

NCT ID: NCT02652728 Not yet recruiting - Heart Failure Clinical Trials

Orodispersible Minitablets of Enalapril in Children With Heart Failure Due to Dilated Cardiomyopathy

LENA-WP08
Start date: January 2016
Phase: Phase 2/Phase 3
Study type: Interventional

Paediatric clinical trial in 50 children, from 1 month to less than 12 years of age, suffering from heart failure due to dilated cardiomyopathy, to obtain paediatric pharmacokinetic and pharmacodynamic data of enalapril and its active metabolite enalaprilat while treated for 8 weeks with enalapril in form of Orodispersible Minitablets (ODMTs), to describe the dose exposure in this patient population.

NCT ID: NCT02652273 Not yet recruiting - Clinical trials for Arthritis, Rheumatoid

Inhibition of Co-Stimulation in Rheumatoid Arthritis

ICoSRA
Start date: January 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to use abatacept as a clinical molecular probe to evaluate the effects of inhibiting costimulation on immune responses in patients with rheumatoid arthritis (RA).

NCT ID: NCT02626897 Not yet recruiting - Sarcoidosis Clinical Trials

A Comparison of Accelerometers for Measuring Daily Activity in Sarcoid

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

This cross-over study of 12 patients with sarcoidosis will look at two different widely-used accelerometer devices. These devices are wrist worn and similar in size to a wrist-watch. They measure daily activity levels. The investigators hope to use one of these devices in the future within a randomised-controlled trial looking at using methylphenidate for the treatment of sarcoidosis-associated fatigue. In order to ensure that the investigators choose the ideal device the investigators wish to compare the GENEActiv and ActiGraph GT3X devices. Participants will be required to wear the devices for 7 days each, with 6 patients beginning with the GENEActiv device and changing to the ActiGraph device after 7 days, the remaining 6 participants starting with the Actigraph before changing to the GENEActiv. Patients will complete a short exit questionnaire about their experience with the devices and their preference. The best device will be determined by both patient preference and reliability of collecting data.

NCT ID: NCT02623686 Not yet recruiting - Sleep Deprivation Clinical Trials

The Effect of an Aromatherapy Intervention on Sleep in the ICU

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

It is known from the literature that patients in the Intensive Care Unit do not get enough sleep impacting on short and longterm recovery (Tembo & Parker, 2009; Bihari et al, 2012; Kamdar et al, 2012). The use of non-pharmacological interventions such as massage with essential oils is supported by the literature as being useful in encouraging sleep (Richards et al, 2003; Matthews, 2011). Over 30% of cancer patients are accessing complementary therapies such as these (Rees et al, 2000; Lewith et al, 2002). We propose investigating whether aromatherapy massage and the use of essential oils in the form of an Inhalation Patch (Bioesse TM) prove to be a useful intervention for improving patient sleep whilst on the critical care unit.

NCT ID: NCT02621723 Not yet recruiting - Clinical trials for Hospital Readmission

Capturing Readmission Internationally to Prevent Readmission by Safer@Home Group

CURIOS@
Start date: January 2016
Phase: N/A
Study type: Observational [Patient Registry]

CURIOS@ is a prospective multi-centre cross-sectional study to investigate readmissions in participating units. The data collected is derived from two clinical episodes: the episode containing the re-admission and the previous admission (index admission). The main aims are: Outcomes: - Risk factors to predict preventable readmissions in non-surgical patients - Percentage of subjectively non-preventable and preventable readmissions from patient, carer, their nurses and their physician's point of view - Comparison for risk factors on readmissions throughout Europe - Increasing awareness and knowledge for health-care workers on readmissions and its preventability

NCT ID: NCT02603627 Not yet recruiting - Lung Cancer Clinical Trials

Prevalence of COPD in Our Lung Cancer Population, Compared to Controls

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

This study will investigate the prevalence of chronic obstructive pulmonary disease (COPD) in patients who are newly diagnosed with lung cancer and compare it to the prevalence of COPD in controls recruited from a smoking cessation clinic.

NCT ID: NCT02583204 Not yet recruiting - Breast Cancer Clinical Trials

Taxane Chemotherapy and Nail Toxicity in Women With Breast Cancer; Stage Two: Evaluation of Interventions

Start date: October 2015
Phase: N/A
Study type: Interventional

The study compares three strategies to prevent/minimise nail problems occuring in women, with breast cancer, undergoing Taxane chemotherapy. The strategies are: application of nail polish and normal care; application of Onicolife drops and normal care and; normal care only.

NCT ID: NCT02550600 Not yet recruiting - Clinical trials for Acute Respiratory Distress Syndrome

Extracorporeal Lung Assist Device in Acute Lung Impairment

EXODUS
Start date: November 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effect of interventional Lung Assist iLA activve to standard therapy in mechanically ventilated patients with severe acute lung impairment. Hypothesis: iLA(active) reduces the incidence of an increase in SOFA-Score of ≥3 points (or death) within 28 days compared to standard treatment.

NCT ID: NCT02548702 Not yet recruiting - Type 2 Diabetes Clinical Trials

Community-based Sport Programme and Type 2 Diabetes

Fit4Life
Start date: October 2015
Phase: N/A
Study type: Interventional

The Fit4Life intervention aims to engage inactive patients with type 2 diabetes in a community-based sport intervention, with the aim being that all participants complete 1 x 30 min session of physical activity/exercise per week across the 12 months they are involved in the intervention (total study duration 3 years). The aim of the Fit4Life intervention is to slow the progression of disease symptoms and to improve quality of life in those diagnosed with type 2 diabetes. The aim of this research study is thus to evaluate the effectiveness of the intervention in achieving these aims. The hypothesis is that involvement in the Fit4Life programme will increase physical activity, reduce type 2 diabetes disease symptoms and enhance self-reported quality of life in male and female patients aged 35-64.