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NCT ID: NCT00435786 Completed - Diabetes Clinical Trials

Diabetic Patients With End-Stage Renal Disease

Start date: n/a
Phase: N/A
Study type: Observational

In diabetic patients with end-stage renal disease to investigate the prevalence of diabetic complications and quality of life and to compare with non-diabetic patients with ESRD and diabetic patients with normal kidney function.

NCT ID: NCT00437723 Completed - Anemia Clinical Trials

A Study of NeoRecormon in Patients With Chronic Kidney Disease.

Start date: n/a
Phase: Phase 4
Study type: Interventional

This 2 arm study will compare the level of anemia, and the decline in renal function, between patients receiving NeoRecormon, and those not receiving it. Patients with chronic kidney disease, stage 2-4, and not receiving dialysis, will be randomized 2:1 to a group receiving NeoRecormon (at a dose determined by the investigator to achieve and maintain an Hb level of 120-135 g/L), or to a control group not receiving NeoRecormon. The anticipated time on study treatment is 3-12 months, and the target sample size is <100 individuals.

NCT ID: NCT00439257 Completed - Multiple Sclerosis Clinical Trials

Costs, Quality of Life and Functional Outcomes in Veterans Treated for Multiple Sclerosis With Beta-Interferon l-B (Betaseron)

Start date: n/a
Phase: N/A
Study type: Observational

The treatment of multiple sclerosis was evolving in light of specific drug therapies to treat the disease, refinements and acceptance of imaging with MRI to diagnose and monitor the disease process, and progress in understanding the pathogenesis of the inflammatory demyelinating process. The result was to raise new issues in the treatment of the disease, which are then being addressed by studies, including when to initiate treatment and the treatment of partial responders to existing therapies. Paralleling strides in treatment, and of particular importance to the Veterans Administration, was the effectiveness of such therapies, both in terms of cost to the VA Health Care System and quality of life of veterans with multiple sclerosis. This study addressed these issues.

NCT ID: NCT00439322 Completed - PTSD Clinical Trials

Post Traumatic Stress Disorder Among VA Ambulatory Care Patients

Start date: n/a
Phase: N/A
Study type: Observational

Posttraumatic stress disorder (PTSD) occurs in response to an extreme traumatic stressor. It is estimated that as many as 1 million VA patients who were exposed to combat may have PTSD. VA patients with PTSD recently have been designated as a �Special Emphasis� population for which health care resources are allocated at approximately 14 times those allocated to patients without such chronic, complex, and intensive health care needs (i.e., �Basic Care� groups). Despite recognition of its substantial impact upon VA resources, the extent and means by which PTSD affects health and health care use remain unclear. This study seeks to enhance understanding of both the extent and means by which PTSD affects the health and the health care use of patients in VA ambulatory care. To meet this goal, we build on an ongoing HSR&D project, the Veterans Health Study (VHS), a prospective longitudinal study of 2,425 VA ambulatory care patients.

NCT ID: NCT00440960 Completed - Lung Cancer Clinical Trials

Anesthesia in Flexible Bronchoscopy for Lung Cancer Diagnostic

Start date: n/a
Phase: Phase 4
Study type: Interventional

The objective of the study was to establish which anesthetic procedure used during flexible bronchoscopy has the lowest index of complications.

NCT ID: NCT00441402 Completed - Healthy Clinical Trials

Exercise Amenorrhea Stress and Bone Health in Adolescents

Start date: n/a
Phase: N/A
Study type: Observational

This study investigates the role of energy balance and stress in the regulation of hypothalamic-pituitary-gonadal axis in adolescent girls across the fitness spectrum.

NCT ID: NCT00442273 Completed - Dry Eye Syndrome Clinical Trials

Comparison of Autologous Serum and Umbilical Cord Serum Eyedrops for Dry Eye Syndrome

Start date: n/a
Phase: N/A
Study type: Interventional

To compare the therapeutic effect between autologous serum and umbilical cord serum eyedrops in the treatment of severe dry eye syndrome.

NCT ID: NCT00443222 Completed - Refractory Myositis Clinical Trials

Treatment With TNF Blockade, Infliximab, in Patients With Myositis

Start date: n/a
Phase: Phase 2/Phase 3
Study type: Interventional

This is a 4 month open trial with TNF-blockade using infliximab (an antibody that blocks TNF) in adult patients with chronic myositis (polymyositis, dermatomyositis, inclusion body myositis) who have persisting muscle weakness and inflammatory active disease despite adequate treatment with immunosuppressives either currently or previously. Infliximab is given as infusions, 5 mg/kg body weight, these infusions are repeated after 2, 6 and 14 weeks. The study involves 15 adult patients. Primary outcome measure is muscle function assessed by muscle function index score. Other outcome measures are Myositis Disease Activity core set: Patient’s global assessment and physicians global assessment on visual analogue scales (VAS). Manual muscle test, Health assessment questionnaire (HAQ), serum levels of CPK, LD and extra muscular disease activity score. Muscle biopsy, Magnetic resonance imaging (MRI) of thigh muscles and Health related Quality of life, measured by SF-36.

NCT ID: NCT00443742 Completed - Depression Clinical Trials

Diagnosis of Depression Among Adolescents

Start date: n/a
Phase: N/A
Study type: Observational

The objective of the study is to improve general practitioners' diagnoses of adolescent depression. Major depression is ranked fourth in the worldwide disability impact. The proportion of adolescents suffering from depressive disorders also seems to be increasing worldwide. Early interventions are known to reduce this illness. Therefore, the earlier depression can be identified in adolescents, the greater the advantage.

NCT ID: NCT00444483 Completed - Metabolic Control Clinical Trials

Structured Patient Education and Quality of Life of Elderly Patients With Diabetes Mellitus- a Prospective Study

Start date: n/a
Phase: N/A
Study type: Interventional

The improvement of the quality of life (QoL) is one of the key treatment goals in patients with diabetes mellitus. Objective: Prospective study to evaluate the impact of structured diabetes education on the QoL in insulin-treated, elderly patients with type 2 diabetes mellitus. Inpatients with insulin treated type 2 diabetes or failure of oral antidiabetic therapy were successively recruited and participated in the structured inpatient diabetes treatment and teaching program (DTTP) for insulin therapy QoL was assessed before and six months after participation in the DTTP with the standardised questionnaire of Lohr analysing the subscales: social relations, physical complaints, worries about the future, diet restrictions, fear of hypoglycemia, and daily struggles.