Clinical Trials Logo

Filter by:
NCT ID: NCT02451943 Active, not recruiting - Soft Tissue Sarcoma Clinical Trials

A Study of Doxorubicin Plus Olaratumab (LY3012207) in Participants With Advanced or Metastatic Soft Tissue Sarcoma

ANNOUNCE
Start date: September 14, 2015
Phase: Phase 3
Study type: Interventional

The main purpose of this study is to evaluate the efficacy of the combination of doxorubicin plus the study drug known as olaratumab versus doxorubicin plus placebo in participants with advanced or metastatic soft tissue sarcoma.

NCT ID: NCT02440776 Active, not recruiting - Cluster Headache Clinical Trials

Pathway CH S&E Registry

SER
Start date: April 2015
Phase:
Study type: Observational [Patient Registry]

Monitor the safety and performance of the Pulsante Microstimulator System.

NCT ID: NCT02439229 Active, not recruiting - Bone Development Clinical Trials

The Vitamin D and Fetal Bone Length Study (VITFBL)

Start date: January 2010
Phase: N/A
Study type: Observational [Patient Registry]

The Vitamin D and fetal bone length study: Vitamin D and its association to bone length in midterm pregnancy.

NCT ID: NCT02439073 Active, not recruiting - Lung Cancer Clinical Trials

Postoperative Rehabilitation in Operation for LUng CAncer (PROLUCA)

PROLUCA
Start date: April 2014
Phase: N/A
Study type: Interventional

Purpose The purpose of the PROLUCA study is to investigate the efficacy of early postoperative rehabilitation in a non-hospital setting in patients with operable lung cancer, with focus on exercise training. Design/Methods One hundred and twenty-eight (n=128) participants (64 patients/study arm) with Non-Small Cell Lung Cancer (NSCLC), stage I-IIIa, referred for surgery, will be randomized to one of the following two groups: 1. Early postoperative rehabilitation initiated as early as two weeks after surgery 2. Postoperative rehabilitation initiated 14 weeks after surgery Intervention The intervention consists of a supervised group exercise program comprising resistance and cardiorespiratory exercise two hours weekly for 12 weeks combined with individual counseling. The primary study endpoint is Maximal oxygen uptake measured by a VO2peak test (direct measurement) Secondary endpoints include: Six minutes walk distance (6MWD), One-repetition-maximum (1RM) Patient-reported outcomes (PROs) on health related quality of life, fatigue, depression, lifestyle, postoperative complications, hospitalization time, sick leave, work status and survival. Results The results of PROLUCA will identify the optimal timing of postoperative rehabilitation in NSCLC patients with focus on increasing physical capacity and health related quality of life and reducing the side effects from the treatment of the cancer disease.

NCT ID: NCT02438839 Active, not recruiting - Rectal Cancer Clinical Trials

Curative Chemoradiation of Low Rectal Cancer

WW2
Start date: September 2015
Phase:
Study type: Observational

The aim of the present study is to investigate whether curative chemoradiation of low rectal cancer is feasible, safe and effective in a multicenter study with results comparable to those of single center studies. Results from previous studies indicate that a considerable fraction of patients with low rectal cancer can be cured by a combination of radiation and chemotherapy alone and thus be spared from operation.

NCT ID: NCT02434900 Active, not recruiting - Clinical trials for Abortion, Spontaneous

Vitamin D and Angiogenic Markers in Odense Child Cohort 1

VITAM
Start date: January 2010
Phase: N/A
Study type: Observational [Patient Registry]

The Vitamin D and Angiogenic Marker Study 1: Vitamin D and angiogenic markers in early pregnancy. Epidemiology and associations to early-pregnancy miscarriage

NCT ID: NCT02433327 Active, not recruiting - Clinical trials for Paediatric Early Warning System

Paediatric Early Warning System - A Danish Multi-center Study

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

Critical illness in the patient and death can potentially be predicted and prevented. Deterioration of the clinical condition of hospitalised patients is often preceded by physiological changes up to 24 hours before death. Despite this several reports show that lack of identification and proper actions in patients developing acute and critical illness remains a problem. The purpose of this study is to investigate if Paediatric early Warning Score (PEWS) optimises identification of acute and critically ill children and prevents life-threatening situations. The hypothesis is that implementation of PEWS supported by directions for action algorithms for intervention will have an impact on number of unplanned transfers to intensive care in already hospitalised children. This study is a multi-centre randomised controlled intervention study designed within a Complex Intervention framework; the study sheds light on the problem, validation of the data collection instrument, testing of the intervention and evaluation. The study involves all paediatric departments and some acute departments in Central Denmark Region. The study is designed as a randomised controlled intervention study where children are randomised to one of two different Paediatric Early Waning Score models. Development and implementation of PEWS is expected to contribute to reduce the number of children developing acute critical illness, number of admissions to intensive care. PEWS is also expected to contribute to increase professional skills and competences in health professionals. It is expected that this study will contribute towards working with a joint PEWS model in Denmark. Last but not least it must be expected that a PEWS model will contribute to reducing the costs for society as an intensive care hospital bed is more expensive than a hospital bed at a general paediatric department.

NCT ID: NCT02431338 Active, not recruiting - Clinical trials for ST-elevation Myocardial Infarction

Cost-effectiveness of Remote Ischemic Conditioning as an Adjunct to Primary Percutaneous Coronary Intervention

Start date: February 2007
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the cost-effectiveness of remote ischemic conditioning as an adjunct to primary percutaneous coronary intervention from the perspective of a Danish healthcare system.

NCT ID: NCT02426307 Active, not recruiting - Clinical trials for Aortic Valve Stenosis

Subclinical Aortic Valve Bioprosthesis Thrombosis Assessed With 4D CT

SAVORY
Start date: April 2015
Phase:
Study type: Observational

TAVR is an increasingly used technique for the treatment of aortic valve stenosis. However, recent clinical experience has suggested that subclinical aortic valve bioprosthesis thrombosis may occur early after valve replacement. The frequency of this potentially ominous phenomenon on both transcatheter and surgical aortic valve bioprosthesis is unknown, as this condition is difficult to detect. The recent development of cardiac 4D computed tomography imaging (4DCT) shows great promise for the evaluation of valve leaflet mobility and morphology. The purpose of this study is in an observational design to assess the frequency of subclinical abnormal leaflet motion and morphology in patients treated with transcatheter or surgical aortic valve bioprosthesis. In addition, the 'natural evolution' of this phenomenon as well as its relation to medical treatment and MACCE will be assessed.

NCT ID: NCT02420054 Active, not recruiting - Obesity Clinical Trials

Short Term Intermittent Fasting and Insulin Resistance

IFAST
Start date: April 2015
Phase: N/A
Study type: Interventional

The purpose of the study is to determine the effect of intermittent fasting on insulin secretion and insulin sensitivity in skeletal muscle and fat distribution.