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NCT ID: NCT01479946 Withdrawn - Breast Cancer Clinical Trials

Electrochemotherapy For The Treatment Of Breast Cancer That Has Spread to the Skin

Start date: October 2011
Phase: Phase 2
Study type: Interventional

Electroporation combined with chemotherapy (ECT) has been shown to be an effective treatment for breast cancer that has spread to skin. In routine clinical practise, ECT is offered to patients when all other treatment options have been exhausted. This study tests the hypothesis that early treatment with ECT may result in improved local control of skin metastases, improved quality of life and reduced health care costs. Patients are randomised to either ECT given as early as possible in the course of the disease or delaying ECT for at least 6 months.

NCT ID: NCT01413854 Withdrawn - Depression Suicidal Clinical Trials

Diclofenac add-on to Treatment as Usual for Suicidal Patients

Start date: August 2011
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine whether diclofenac is effective in the treatment of depressed patients with a recent suicide attempt.

NCT ID: NCT01412840 Withdrawn - Pain Clinical Trials

Sterile Water Injections for Relieving Ureterolithiasis Pain

Start date: January 2014
Phase: N/A
Study type: Interventional

Ureterolithiasis pain is a severe condition for which it takes some 30 minutes for standard treatment to yield maximal pain relief, a period during which the patient suffers severe to intolerable pain. It would thus be valuable to further evaluate sterile water injection as a method for achieving rapid relief for this type of pain.

NCT ID: NCT01294904 Withdrawn - Infertility Clinical Trials

Mechanisms of Infertility and Hormonal Changes in Patients With Chronic Kidney Disease

Start date: January 2011
Phase:
Study type: Observational

Patients with chronic kidney disease (both men and women), especially those with terminal renal failure, manifest infertility. There has been demonstrated several hormonal changes in patients on dialysis. Increased levels of luteinizing hormone (LH) has been seen in men (12). In women the opposite has been reported. The number of spermatocytes is reduced and a disturbance in maturation has been observed. This project is aimed to study the influence of uremic milieu on fertility in men and women. The hypopituitary/hypothalamus gland axis and hormonal levels will be studied.

NCT ID: NCT01223066 Withdrawn - Clinical trials for Females Recently Treated With Macrolane VRF in the Breasts

Macrolane Prospective Survey

Start date: September 2010
Phase:
Study type: Observational

The study objective is to evaluate the long term safety when Macrolane Volume Restoration Factor is used in female breasts in clinical practice.

NCT ID: NCT01214122 Withdrawn - Pharmacokinetics Clinical Trials

A Drug-Drug Interaction Study Between AZD9668 and Warfarin to Study the Effect of AZD9668 on the Metabolism and Effect of Warfarin

Start date: November 2010
Phase: Phase 1
Study type: Interventional

The primary purpose of this study is to determine whether the treatment with AZD9668 will affect the metabolism and effect of Warfarin.

NCT ID: NCT01187576 Withdrawn - Clinical trials for Motivation for Physical Activity

A Multi-professional Team Intervention on Physical Activity Referrals in Primary Care Patients With Cardiovascular Risk Factors—the Dalby Lifestyle Intervention Cohort (DALICO) Study

DALICO
Start date: November 2010
Phase: N/A
Study type: Interventional

Background The present study protocol describes the trial design of a primary care intervention cohort study, which examines whether an extended, multi-professional physical activity referral (PAR) intervention is more effective in enhancing and maintaining self-reported physical activity than ordinary physical activity recommendations. The study targets patients with newly diagnosed hypertension and/or type 2 diabetes. Secondary outcomes include: need of pharmacological therapy; blood pressure/plasma glucose; physical fitness and anthropometric variables; mental health; health related quality of life; and cost-effectiveness. Methods/Design The study is designed as a long-term intervention. Three primary care centres are involved in the study, each constituting one of three treatment groups: 1) Intervention group (IG): multi-professional team intervention with PAR, lifestyle brochure; 2) Control group A (CA): ordinary recommendations on health behaviours, lifestyle brochure; and 3) Control group B: treatment as usual (retrospective data collection). The intervention is based on self-determination theory and follows the principles of motivational interviewing. Physical activity is measured with the International Physical Activity Questionnaire (IPAQ) and expressed as metabolic equivalent of task (MET)-minutes per week. Physical fitness is estimated with the 6-minute walk test in IG only. Variables such as health behaviours; health-related quality of life; motivation to change; mental health; demographics and socioeconomic characteristics are assessed with an electronic study questionnaire that submits all data to a patient database, which automatically provides instant feed-back on the patients' health status. Cost-effectiveness of the intervention is evaluated continuously and the intermediate - 3 - outcomes of the intervention are extrapolated by economic modelling. The first statistical analyses and compilation of results will be performed one year after inclusion of the first patient or when the IG and CA have included 60 and 30 eligible patients respectively. Discussion By helping patients to overcome practical, social and cultural obstacles and increase their internal motivation for physical activity we aim to improve their physical health in a long-term perspective. The targeted patients belong to a patient category that is supposed to benefit from increased physical activity in terms of improved physiological values, mental status and quality of life, decreased risk of complications and maybe a decreased need of medication.

NCT ID: NCT01119547 Withdrawn - Osteoarthritis Clinical Trials

Patient Education Program for Osteoarthritis With Exercise Included

PEPOA-E
Start date: September 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate if inclusion of exercise in an education program for patients with osteoarthritis can improve self efficacy, self-perceived health and function.

NCT ID: NCT01087411 Withdrawn - Overweight Clinical Trials

Intervention Study to Prevent Obesity in Sedentary 8 Year Old Swedish Children

STOPP-8
Start date: October 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to study whether a targeted intervention can increase physical activity in inactive 8-yr old children and how it affects secondary measures such as metabolic- and cardiovascular risk factors and markers, self-reported quality of life, BMI, body composition and aerobic work-capacity.

NCT ID: NCT01022983 Withdrawn - Heart Failure Clinical Trials

Preoperative Levosimendan and Heart Failure

PELS
Start date: April 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate the safety and efficacy of Levosimendan given preoperative to patients with heart failure undergoing noncardiac surgery.