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Elderly clinical trials

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NCT ID: NCT00748683 Completed - Elderly Clinical Trials

Development of an Integrated Health Care Environment for Elderly With RFID Technology

Start date: September 2008
Phase: Phase 0
Study type: Interventional

A falling prevention system will be established by RFID location and motion detection. - Using RFID to detect participants' allocation indoor. - Modifying environment parameters such as light, sound, to alert users if them enter a place with potential hazards. Data exchange models will also developed in this project - Interchanging different data including physiological data and RFID data into a database - establishing interchange protocol according the HL7 standard

NCT ID: NCT00738816 Completed - Elderly Clinical Trials

Effect of Systematic Medication Review in Elderly Patients Admitted to an Orthopedic Department

Start date: April 2009
Phase: N/A
Study type: Interventional

Elderly patients have a higher risk of experiencing adverse drug events due to an age related increase in morbidity and medication use. Inappropriate or wrong medication use among elderly patients acutely admitted to hospitals is assumed to result in earlier contact to general practitioner, emergency departments and re-admissions if not corrected during hospital admission. It is therefore our hypothesis that a systematic medication review conducted by pharmacists and physicians specialized in pharmacology will increase time to first unscheduled physician contact (general practitioner, emergency departments, ambulatory care and re-admissions) after discharge from hospital from an average of 21days to 25 days. Further, the following secondary outcome parameters will be measured at discharge and within 3-month follow-up: - length of in-hospital stay - number of contacts to general practitioner 30 days after discharge, that resulted in medication changes - number of re-admissions at 3-month - number of death at 3-month - number of contact to primary health care at 3-month - patients self-experienced quality of health(EQ-5D) 3-month

NCT ID: NCT00736762 Completed - Healthy Clinical Trials

Effects of Global Postural re-Education Program

Start date: February 2008
Phase: N/A
Study type: Interventional

The postural alterations present in the seniors people act as predisponent form of incapacities that provoke alterations in the quality of life. The objective of this study is to evaluate the biomechanical characteristics of the balance of elderly people, before and after treatment with Global Postural Re-education. This research is characterized by experimental method of investigation.Thirty elderly people (30 women) will be randomized to two different groups from Group of Studies of Third Age - GETI, at University of the State of Santa Catarina: - fifteen elderly women will be submitted to the Global Postural Re-education (GPR) program and to the GETI program of activities - fifteen elderly women will be submitted only to the GETI program of activities. At baseline the subjects will be screened for balance measurements with the chattecx balance system and Berg Scale. These measurements will be repeat immediately after the intervention. The subjects randomised to the GPR program will participate in posture retraining techniques of approximately forty minutes, one time a week for ten weeks. The independent t test for pairs of random samples will be used, with level of significance of p≤0,05.

NCT ID: NCT00736528 Terminated - Healthy Clinical Trials

A Phase I, Multiple Dose Study of PF-04447943 in Healthy Elderly Volunteers

Start date: August 2008
Phase: Phase 1
Study type: Interventional

To describe the safety, tolerability and pharmacokinetics of PF-04447943 after administration of multiple, ascending, oral doses to healthy elderly subjects.

NCT ID: NCT00733161 Completed - Clinical trials for Congestive Heart Failure

Effect of Passive Exercise on Systemic Endothelial Function in Elderly Patients With Chronic Heart Failure

Start date: August 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the effect of passive exercise on systemic endothelial function in elderly patients with chronic heart failure.

NCT ID: NCT00728520 Recruiting - Clinical trials for Acute Myeloid Leukemia

Trial With Azacitidine in Newly Diagnosed Acute Myelogenous Leukemia (AML) Veterans Administration (VA) Elderly Patients Not Eligible for Standard Induction Therapy

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

The drug that will be used in this study is called Azacitidine. Azacitidine belongs to a group of drugs which may restore normal control in cancer cells by affecting the genes and proteins in the body. Azacitidine is approved by the FDA for the treatment of Myelodysplastic Syndrome (MDS), a pre-leukemic bone marrow disease. The purpose of this study is to find out what effect the drug Azacitidine has on Acute Myeloid Leukemia (AML) in elderly patients.

NCT ID: NCT00725166 Completed - Sarcopenia Clinical Trials

Human Muscle Gene Expression Profiles in Young and Old Men

CERA
Start date: October 2008
Phase: N/A
Study type: Observational

To reach the goals of living longer in better medical conditions, many countries reach the same conclusion: new strategies have to be developed to avoid, or at least limit, the effects of age; this requires a better knowledge of the mechanisms of aging. Our project focuses on the loss of muscle mass associated with aging, called sarcopenia. Sarcopenia unavoidably leads to impaired mobility and poor balance, which contributes to loss of functional autonomy and to increased prevalence for severe falls. Skeletal muscle also plays a central role as a reserve for energy and amino acids. Hence, sarcopenia further triggers severe side metabolic effects such as frailty among elderly persons. The precise mechanisms of muscle aging are still mostly unknown, although many theories have been proposed. The present study aims at better understanding the mechanisms of skeletal muscle loss associated with aging. Using muscle biopsies from young and old subjects, the differential expression profiles of mRNA will be obtained through chips that will evaluate more than 39000 transcripts. On the same samples, proteomic analyses will involve two complementary approaches: (1) bidimensional electrophoresis (2DGE) coupled to mass spectrometry (MALDI-ToF) for dominant proteins; (2) Western-blot (more than 800 antibodies) targeting regulating proteins not detectable using 2DGE. Complementary histological studies (immunohisto-fluorescence, confocal microscopy) will specify the localisation of the major biomarkers in the muscle biopsies. The results of that research will have applications in the medium term and will lead to nutritional interventions to modulate specific metabolic pathways and improve the quality of life in the elderly.

NCT ID: NCT00719953 Completed - Elderly Clinical Trials

Study to Assess the Efficacy of Cognitex

Cognitex001
Start date: August 2008
Phase: Phase 4
Study type: Interventional

A Single-Center, Open Label Study to Assess the Efficacy of Cognitex in Elderly Subjects with Memory Impairment

NCT ID: NCT00714675 Completed - Elderly Clinical Trials

Citrulline and Protein Metabolism in the Malnourished Elderly People

CIPROAGE
Start date: December 2009
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the effects of a supplementation of citrulline for three weeks in elderly malnourished and hospitalised subjects on muscle protein synthesis.

NCT ID: NCT00589082 Completed - Elderly Clinical Trials

DaunoXome + Ara-C vs Daunorubicin + Ara-C in Elderly AML

Start date: October 2001
Phase: Phase 3
Study type: Interventional

Overall results in the treatment of middle aged adults acute myelogenous leukemia (AML) are substantially improved in the last decade, with complete remission (CR) rates established to values of 70 to 80per cent and also encouraging long-term outcome, especially in patients who can tolerate intensified post remissional treatment strategies. On the contrary, there has been little progress in the treatment of older patients. In these patients the response rate generally range between 40 and 60per cent, and overall survival at 2 years is often less than 10 per cent. Usually, a combination of anthracyclines daunomycin DNR or doxorubicin and cytarabyne Ara-C has been utilized for the remission-induction treatment, with schedules similar to those utilized in younger cases, for patients eligible to intensive treatments. Variation of the dose of DNR has not brought any significant benefit. The EORTC HOVON randomized trial AML9 compared two drugs in induction for previously untreated patients. DNR versus Mithoxantrone (MTZ). MTZ induction therapy produces a slightly better CR rate than DNR-containing regimen (47per cent vs 38per cent, P equals 0.069), without any significant effect on remission duration and survival. The DFS probability between the two treatment arms was not different. The median DFS estimates were 39 weeks in both groups. The DFS rate at 5 years was 8per cent. Also the duration of survival was similar (p equals 0.23) in the two treatment groups. Median survival estimates were 36 weeks (DNR) and 39 weeks (MTZ). The percentage of patients still alive at 5 years were 6per cent and 9per cent respectively.