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NCT ID: NCT02493868 Completed - Clinical trials for Depressive Disorder, Treatment-Resistant

A Study of Intranasal Esketamine Plus an Oral Antidepressant for Relapse Prevention in Adult Participants With Treatment-resistant Depression

SUSTAIN-1
Start date: October 1, 2015
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the efficacy of intranasal esketamine plus an oral antidepressant compared with an oral antidepressant (active comparator) plus intranasal placebo in delaying relapse of depressive symptoms in participants with treatment-resistant depression (TRD) who are in stable remission after an induction and optimization course of intranasal esketamine plus an oral antidepressant.

NCT ID: NCT02493400 Completed - Atrial Fibrillation Clinical Trials

Physiotherapist Led Group-exercise Compared Physical Activity on Prescription, a 3 Months Follow-up

Start date: August 2014
Phase:
Study type: Observational

To investigate the effect of exercise or PAP prescription 3 months after completion of the study "Should elderly patients with atrial fibrillation be offered physiotherapist group exercise or can physical activity on prescription (PAP) be used as an alternative?" regarding level of physical fitness, physical activity, heart rate and health related quality of life (HR-QoL). Also if any of the investigated variables can predict the possible change in physical fitness.

NCT ID: NCT02493387 Completed - Atrial Fibrillation Clinical Trials

Supervised Exercise Compared to PAP in Patients With Permanent Atrial Fibrillation

Start date: January 2013
Phase: N/A
Study type: Interventional

Atrial fibrillation is the most common arrhythmia, and physical activity and exercise are sometimes avoided due to symptoms such as palpitations, fatigue and anxiety. Physiotherapist-led group based exercise as part of cardiac rehabilitation is rare for this group of patients, the method physical activity on prescription is used to encourage the patient to increase their physical activity level in order to reduce the risk of premature morbidity and mortality. However, mostly in this method you do not know the patient's ability to perform the prescribed amount of physical activity, and its effect on physical fitness has not been studied in patients with heart disease, neither has the effect of physiotherapist led group-based exercise in patients with atrial fibrillation. The aim was to investigate the impact of physiotherapy led group-based exercise compared to physical activity on prescription in patients with atrial fibrillation regarding the level of physical fitness, physical activity, heart rate and health related quality of life (HR-QoL).

NCT ID: NCT02492191 Completed - Clinical trials for Postoperative Complications

RAPP- Systematic E-assessment of Postoperative Recovery in Patients Undergoing Day Surgery

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

Introduction Day surgery is a well-established practice in many European countries, but only limited information is available regarding postoperative recovery at home though there is a current lack of a standard procedure regarding postoperative follow-up. Furthermore, there is also a need for improvement of modern technology in assessing patient related outcomes such as native software applications. This article describes the RAPP study protocol, a mixed-methods study to evaluate if a systematic e-assessment follow-up in patients undergoing day surgery is cost effective and improves postoperative recovery, health and quality of life. Methods and analysis This study is a mixed-methods study design that includes a multicenter, two-group, parallel, single-blind randomized controlled trial (RCT) and qualitative interview studies. One thousand patients >17 years of age who are undergoing day surgery will be randomly assigned to either e-assessed postoperative recovery follow-up daily in 14 days measured via smartphone app including the Swedish web-version of Quality of Recovery (SwQoR) or to standard care (i.e. no follow up). The primary aim is cost effectiveness. Secondary aims are improvements on postoperative recovery, health-related quality of life (QoL) and overall health; (b) to determine whether differences in health literacy have a substantial and distinct effect on postoperative recovery, health, and QoL; and (c) to describe day-care patient and staff experiences with a systematic e-assessment follow-up after day surgery.The primary will be measured at 2 weeks postoperatively and secondary outcomes b) at 1 and 2 weeks and c) at 1 and 4 months.

NCT ID: NCT02491593 Completed - Clinical trials for Colorectal Neoplasms

Quantitative Immunochemical Fecal Occult Blood Test in Symptomatic Patients

FIKA
Start date: April 2014
Phase:
Study type: Observational

The aim of this study is to compare the outcome of three (3) quantitative immunochemical faecal occult blood test in symptomatic patients.

NCT ID: NCT02491580 Completed - Neoplasms Clinical Trials

Post-transplant Cancer Incidence and Survival in Patients With or Without Pre-transplant Cancer

Start date: October 2014
Phase: N/A
Study type: Observational

Patients with previous malignancies have increasingly been accepted for renal transplantation. However, post-transplant malignancy risk and survival rates of these patients are unknown. Our aim was to assess if previous malignancies pose an unnecessarily high risk of post-transplant malignant tumours and if the organs as a resource are too limited for investment in this patient group.

NCT ID: NCT02487043 Completed - Clinical trials for Early Childhood Caries

A Telephone-based Case-management Intervention for Caries Prevention in Children With Severe Early Childhood Caries

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

Despite improvements in oral health among children, children living in areas characterized by low socio-economic status still have a significant disease burden with regard to dental caries. Special efforts to prevent disease development in this group of children have been unsuccessful. Small children with extensive treatment needs often have limited abilities to cooperate and to provide quality dental care in this patient group, general aneaethesia (GA) may often be the treatment modality of choice. Preschool children treated under general anesthesia have significantly higher caries prevalence (deft and defs), apical parodontitis and infection due to pulpal necrosis. They also have significantly more emergency visits and previous use of treatment under sedation. This study aim to test the hypothesis, that a telephone based case management intervention for children with severe early childhood caries can prevent further caries development in preschool children who are treated under general anesthesia for severe early childhood caries.

NCT ID: NCT02485405 Completed - Stress Clinical Trials

Gut Permeability and Stress

SP15
Start date: June 2015
Phase: N/A
Study type: Observational

The purpose of this study is to analyse gut permeability and stress.

NCT ID: NCT02479607 Completed - Breast Cancer Clinical Trials

Effects of an ICT-platform for Assessment and Management of Patient-reported Symptoms During Treatment for Breast Cancer

PhONEME
Start date: June 30, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effects of an interactive Information and Communication Technologies (ICT) -platform for use in a smartphone or tablet in patients treated with neoadjuvant chemotherapy for breast cancer. The hypothesis is that clinical management will be improved and costs reduced and safe and participatory care promoted, when patients report symptoms in an application which provides self-care advice and instant access to professionals.

NCT ID: NCT02479334 Completed - Healthy Clinical Trials

Acute Effects of Spices on Pathways Associated With Glucose Homeostasis and Inflammation on PBMCs of Healthy Subjects

Start date: June 2015
Phase: Phase 1/Phase 2
Study type: Interventional

This study aims to investigate the effect of spices on gene expression of pathways associated with glucose homeostasis, oxidative stress and inflammation, in the postprandial phase in healthy human subjects.