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NCT ID: NCT01399463 Not yet recruiting - Clinical trials for Coronary Artery Disease

Pressure-wire Guided PTCA: Drug Eluting Stent Versus Drug Eluting Balloon (WinDEB Study)

Start date: August 2011
Phase: N/A
Study type: Interventional

The aim of the study is to show the safety and efficacy of the SeQuent® Please (Drug Eluting Balloon or DEB) vs. commonly used Drug Eluting Stents in the treatment of small vessel disease and side branches by pressure wire guided percutaneous coronary intervention.

NCT ID: NCT01400061 Not yet recruiting - Obesity Clinical Trials

Relation of Blood-boron Levels With Body Mass Index

Start date: August 2011
Phase: N/A
Study type: Observational

According to our experimental experiences w hypothesized that blood boron levels may be corralated to body mass index.

NCT ID: NCT01400126 Not yet recruiting - Clinical trials for System as Compared to Conventional Water System.

Ultrapure Water System for Hemodialysis Therapy

Start date: August 2011
Phase: N/A
Study type: Observational

We wish to compare the effect of very clean water used for dialysis therapy (i.e ultrapure water) in comparison with the use of conventional water which are used in most dialysis units worldwide. To the best of our knowledge prospective data in that field is sparse.

NCT ID: NCT01405482 Not yet recruiting - Clinical trials for Thoracic Outlet Syndrome

Botulinum Toxin Injections for Thoracic Outlet Syndrome

Start date: August 2011
Phase: Phase 1
Study type: Interventional

Botulinum toxin type A injected into the anterior and middle scalene muscles will reduce the irritation on the neurovascular structures at the interscalene triangle in subjects with TOS. This will lead to reductions in pain and paresthesias, and improvements in function when compared with injection of placebo.

NCT ID: NCT01407250 Not yet recruiting - Clinical trials for Patients With Pathological ECG

PhysioGlove Versus Clinic Electrocardiogram Comparison

CommwellPG
Start date: August 2011
Phase: N/A
Study type: Observational

Comparison of the quality of the outpatient clinic electrocardiogram performed on patients sent to a cardiology consultation with a standard cable and the PhysioGlove-ES electrocardiograms performed in the cardiology clinic.

NCT ID: NCT01409525 Not yet recruiting - Clinical trials for Coronary Artery Bypass Surgery Patients

Rate of Microbial Colonization Over Native Calcified Cardiac Valves

Start date: August 2011
Phase: N/A
Study type: Observational

The purpose of this observational, exploratory study in patients undergoing any cardiac valve replacement or repair is to assess the rate of bacterial colonization over native degenerative calcified cardiac valves.

NCT ID: NCT01412775 Not yet recruiting - Clinical trials for Stress, Psychological

Psychological Group Intervention to Reduce Stress and Burnout Among Cardiac Intensive Care Nurses

Start date: August 2011
Phase: N/A
Study type: Interventional

The study will examine the influence of a Cognitive Behavioral Therapy (CBT) short-term group intervention program on the levels of psychological stress and professional exhaustion experienced by the nursing staff in a cardiac department.

NCT ID: NCT01413477 Not yet recruiting - Clinical trials for Allergic Contact Dermatitis

Nickel Desensitization Using Topical Therapy

Start date: August 2011
Phase: N/A
Study type: Interventional

Nickel contact dermatitis (eczema) is one of the most common allergic conditions affecting the skin. This is a study looking at potentially desensitizing nickel-allergic patients to their allergy using anti-inflammatory ointments applied to the skin (arm). Application of these ointments (ie. modified Vitamin D) has been shown to increase specific immune cells (T regulatory cells), which play a role in preventing immune activation and subsequently inflammation. The investigators propose use of topical anti-inflammatory agents (corticosteroids, modified Vitamin D, or both) may desensitize patients with nickel allergy.

NCT ID: NCT01414439 Not yet recruiting - Clinical trials for Congestive Heart Failure (CHF)

Group Psychotherapy Among Congestive Heart Failure Patients

Start date: August 2011
Phase: N/A
Study type: Observational

This study will examine the efficacy of group therapy utilizing the Existential Approach in heart failure patients when compared to a control group of patients who are waiting for the same group treatment. This comparison will be achieved by measuring changes in the variables studied namely, the levels of psychological distress and levels of psycho-social adjustment.

NCT ID: NCT01418456 Not yet recruiting - Diabetes Clinical Trials

Outcomes of Non-infected Diabetic Foot Ulcers With/Without Antibiotics

KADFUT
Start date: August 2011
Phase: Phase 4
Study type: Interventional

The overall objective is to investigate whether antibiotics in the treatment of clinically clean neuropathic and ischaemic ulcers in diabetic foot patients could reduce the incidence of infection and therefore lead to improved outcomes This is a single centre study in which patients with either type 1 or 2 diabetes mellitus, who consecutively present to the Diabetic Foot Clinic [DFC] with clean neuropathic (NU) or ischaemic (IU) diabetic foot ulcer without clinical signs of infection will be invited to take part and will express their willingness to take part in the study by signing a consent form. - All patients will be treated and followed up in the DFC at King's College Hospital. Patients will be randomised into two groups: an antibiotic group and a control group. - The antibiotic group will receive standard treatment along with antibiotics. - The control group will have standard treatment alone. - Patients from both groups will be reviewed at weekly intervals for a period of 20 weeks. - Patients will be removed from the study if they develop clinical signs of infection or if their ulcer heals prior to 20 weeks but will be followed up via routine practice for eventual outcomes