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NCT ID: NCT01506219 Completed - Fragility Clinical Trials

Geriatrician-performed Comprehensive Geriatric Care in an Outpatient Community Rehabilitation Unit

GCGCCRU
Start date: January 17, 2012
Phase: N/A
Study type: Interventional

Introduction: Older adults with multiple illnesses represent the fastest growing sector of society and make increasing demands on all sectors of the health care system, particularly in outpatient community rehabilitation units due to shorter time of stay in acute care units and hospitals. The aim of this study is to investigate the effect of geriatrician-performed comprehensive geriatric care (CGC) in older people referred to an outpatient community rehabilitation unit. Methods: The study is a prospective randomized controlled trial. Settings: two community care rehabilitation units in Aarhus Municipality, Denmark. Inclusion: persons aged 65 and older from home or hospital. Exclusion: persons who received palliative care or had been assessed by a geriatrician during the past month. Intervention: medical history, physical examination, blood tests, medication adjustment and related treatments performed by a geriatrician. Control: usual care in a community rehabilitation unit. Number of hospital admissions and emergency department (ED) visits (primary outcome), number of GP contacts, activities of daily living, physical and cognitive functioning, quality of life, data on institutionalization, medication status, and mortality are assessed at day 30 and 90 after arrival at the rehabilitation unit. Project status: The outpatient CGC model is developed, implemented and compared with usual care in a pragmatic RCT.

NCT ID: NCT01506180 Completed - Acute Disease Clinical Trials

In-Hospital Comprehensive Geriatric Assessment in Aged Acute Medical Patients

Start date: January 2010
Phase: N/A
Study type: Observational

The purpose of this study is to compare acute ill elderly medical patients in a geriatric department with general medical departments, and to examine the effects of comprehensive geriatric assessment in the geriatric setting compared with general medical care.

NCT ID: NCT01505322 Completed - Pain Clinical Trials

Persistent Pain to Impair Daily Activities Following Thoracic Surgery

Start date: August 2010
Phase: N/A
Study type: Observational

Can pain impairment of daily activities be shown to be procedure specific, and thus used as an alternative to pain scoring.

NCT ID: NCT01504698 Completed - Neck Pain Clinical Trials

Manipulative Treatment of Children With Neck and Back Pain

Start date: February 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effect of manipulative treatment of children with neck and back pain. Because manipulation is the most frequently used treatment of musculoskeletal complaints in children, and an increasing number of Danish children see a chiropractor, it appears obvious to start the search for evidence by examining the effect of this treatment.

NCT ID: NCT01504139 Completed - Infertility Clinical Trials

The Luteal Phase After GnRHa Trigger - a Proof of Concept Study

Start date: January 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate levels of progesterone in the luteal phase after various stimulations in the follicular phase and treatment with GnRH antagonist protocol followed by GnRHagonist as induction of ovulation.

NCT ID: NCT01504009 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Muscle Training of Patients With Amyotrophic Lateral Sclerosis (ALS)

ALS-project
Start date: May 2011
Phase: N/A
Study type: Interventional

Patients with neuropathic diseases are experiencing increasing muscle weakness, loss of muscle strength and functional abilities during their illness. In healthy people, regular exercise is the best way to maintain or improve muscle strength, endurance and general health status and thereby maintain functioning abilities. Previously, patients with neuromuscular diseases were advised to avoid any kind of physical exercise. However, lately a number of studies have evaluated the effect of training in patients with neuromuscular diseases, and positive effects on the functional abilities have been found. Based on these findings we want to investigate the mechanisms leading to development of muscle atrophy and loss of functional abilities, and to explore the opportunities of reducing muscle wasting and thereby improve the course of the disease development through strength training. The main objective is to investigate the effects of strength training on slowing disease progression and reduce the decline in muscle strength and function in patients with amyotrophic lateral sclerosis (ALS). In addition, the aim is to carry out detailed studies of biological processes in muscle tissue in order to unveil mechanisms leading to muscle atrophy, and to examine effects of a strength training program. The goal is to be able to incorporate strength training in the treatment program of these patients in order to maintain muscle strength and function in the individual for as long as possible. Minimum 10 patients with the disease are included in the study. Through a 12 week period the patients will participate in strength training 2-3 times per week. Muscles biopsies will be taken (i) 12 weeks before commencement of strength training program, (ii) at the beginning of training and (iii) after 12 weeks of strength training. Patients will function as their own controls. Blood samples will be collected simultaneously in order to follow the development of the strength training. Furthermore, participants will be assessed through at number of functional tests and questionnaires evaluating their strength, balance and social/ psychological status. Subjects are recruited through their association with Odense University Hospital. In the present study, the participants become part of a social network, while participating in organized training sessions, and thus have a possibility to make contact with other ALS patients in the same situation as themselves.

NCT ID: NCT01502982 Completed - Clinical trials for Diffuse Large B-Cell Lymphoma

Dose Dense Chemotherapy and Rituximab for Young High Risk Diffuse Large B-Cell Lymphoma Patients (CRY-04)

CRY-04
Start date: November 2004
Phase: Phase 2
Study type: Interventional

The purpose is to test whether dose densified chemoimmunotherapy followed by central nervous system (CNS) prophylaxis for young high risk diffuse large B-cell lymphoma (DLBCL) patients is feasible and could improve time to treatment failure and reduce the risk of CNS relapses. Six courses of rituximab-cyclophosphamide-doxorubicin-etoposide-vincristine-prednison (R-CHOEP) given in two weeks intervals with the support of G-CSF is followed by one course of high dose methotrexate (HD-MTX) and high dose cytarabine (HD-Ara-C). The results will be compared to a historical Nordic study.

NCT ID: NCT01500421 Completed - Cerebral Infarction Clinical Trials

Safty and Feasibility Study of Therapeutic Cooling in Acute Ischemic Stroke (COOLAID Øresund)

Start date: October 2008
Phase: Phase 2
Study type: Interventional

This study is designed to investigate the safty and feasibility of therapeutic hypothermia in acute stroke patients. Soon after arrival in the stroke unit patients are randomized to either hypothermia in the intensive care unit (ICU) or standard treatment in the stroke ward. Patients randomized to therapeutic hypothermia are analgo-sedated and cooled to at temperature of 33 degrees for a period of 24 hours.

NCT ID: NCT01499875 Completed - Clinical trials for Phenoxymethylpenicillin

A Pharmacokinetic and Pharmacodynamic Study of Phenoxymethylpenicillin for Children

Start date: January 2012
Phase: Phase 1
Study type: Interventional

The aim of this trial is to evaluate the pharmacokinetics and pharmacodynamics of penicillin V in non-infectious children to estimate the optimum dosage regime in children.

NCT ID: NCT01499641 Completed - Disc Disease Clinical Trials

Epidural Steroid Following Discectomy for Herniated Disc Reduces Morbidity

Start date: May 2001
Phase: N/A
Study type: Interventional

Focus of this study is evaluation of the outcome, neurologic impairment and safety of epidural steroide following lumbar discectomy for herniated disc disease.