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Quality of Life clinical trials

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NCT ID: NCT00270049 Completed - Cancer Clinical Trials

Epoetin Alfa for the Treatment of Anemia Resulting From Chronic Lymphocytic Leukemia

Start date: November 1990
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effect of treatment with epoetin alfa versus placebo on the percentage of red blood cells in anemic patients with chronic lymphocytic (white blood cell) leukemia and its effect on the patients' quality-of-life. Epoetin alfa is a genetically engineered protein that stimulates red blood cell production.

NCT ID: NCT00248989 Completed - Quality of Life Clinical Trials

Effect of DHEA on Skin Aging in Postmenopausal Women

Start date: November 1, 2004
Phase: Phase 3
Study type: Interventional

The purpose of the study is to determine the response of skin parameters related to skin aging to the local action of DHEA in postmenopausal women.

NCT ID: NCT00246597 Terminated - Quality of Life Clinical Trials

A Phase III Clinical Trial of PROCRIT (Epoetin Alfa) Versus Placebo in Women Undergoing Adjuvant Chemotherapy for Stage I, II or III Breast Cancer

Start date: December 2002
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether it is possible to measure temporary difficulty with thinking and/or short-term memory in women who are receiving chemotherapy for early stage breast cancer and to determine whether or not treatment with PROCRIT® will help decrease any problems with thinking or short-term memory that chemotherapy may cause.

NCT ID: NCT00224146 Completed - Quality of Life Clinical Trials

Transdermal (TDS) Oxybutynin (Oxytrol(r)) in Overactive Bladder

MATRIX
Start date: May 2004
Phase: Phase 4
Study type: Interventional

This study evaluates changes in health related quality of life outcomes in patients using Oxytrol(r)

NCT ID: NCT00211133 Completed - Quality of Life Clinical Trials

A Study to Evaluate the Impact of Maintaining Hemoglobin Levels Using Epoetin Alfa in Patients With Metastatic Breast Cancer Receiving Chemotherapy

Start date: June 2000
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the impact on survival and quality of life of maintaining hemoglobin in the range of 12 to 14 g/dL using epoetin alfa or placebo in patients starting chemotherapy for metastatic breast cancer for the first time.

NCT ID: NCT00205517 Terminated - Depression Clinical Trials

Sedation and Psychopharmacology in Critical Care

Start date: September 2002
Phase: N/A
Study type: Interventional

Certain methods of sedation increase the duration of respiratory failure. Two strategies, a nursing- implemented sedation algorithm and daily interruption of sedatives, decrease length of mechanical ventilation compared to "conventional care" but have not been compared to each other. The reason certain methods of sedation lead to prolonged respiratory failure is unknown but may be related to altered pharmacokinetics and dynamics that are unique to critically ill patients. Critically ill patients receive substantial doses of sedatives over prolonged periods. The impact of these management strategies on short- and long-term psychiatric complications are unknown. The study seeks to test the central hypothesis that sedation practices impact strongly on outcome of respiratory failure and psychiatric complications. The three specific aims are (1) to compare two sedation strategies (protocol directed sedation and daily interruption of sedatives), (2) to examine the prevalence of psychiatric complications, and (3) to compute the pharmacokinetics of commonly used sedatives and narcotics. These aims will be achieved by enrolling critically ill patients in a prospective randomized trial comparing the above mentioned sedation strategies, and assessing sedation level as well as delirium throughout the duration of respiratory failure. Sedative plasma levels will be measured, and pharmacokinetics computed. Psychiatric morbidity will be assessed by administration of validated questionnaires.

NCT ID: NCT00184834 Completed - Quality of Life Clinical Trials

Quality of Life and Liver Metastases

Start date: June 1999
Phase: N/A
Study type: Observational

An increasing aggressiveness in the surgical approach of colorectal liver metastases is observed. This seems only justified when, besides prolongation of survival, also the health status of patients is considered. The aim of this prospective study is to investigate the impact of surgery on health-related quality of life in this specific patient population operated for colorectal liver metastases.Furthermore, as the indications for hepatic resection are broadened and patients with more extensive liver disease are operated on, the chance of non operable disease at laparotomy will increase. The effects of such an event on HRQol are also studied.

NCT ID: NCT00182234 Completed - Quality of Life Clinical Trials

SONICS - Effectiveness of Specialist Oncology Nursing

Start date: December 2005
Phase: Phase 3
Study type: Interventional

This research project will address the issue of gaps in continuity of supportive care for cancer patients during the early phases of the disease trajectory that result in unmet needs and unnecessary morbidity. The investigators intend to study the impact of a specialized cancer-nursing program, Interlink Community Cancer Nurses (Interlink) on patient outcomes. Impact will be assessed directly using a validated measure of continuity of care from the patients' perspective and validated measures of key supportive care patient outcomes including unmet needs, distress, uncertainty in illness, and quality of life, in a randomized trial.

NCT ID: NCT00165997 Terminated - Quality of Life Clinical Trials

Quality of Life in Patients Post Radiofrequency Ablation

Start date: February 2004
Phase: N/A
Study type: Observational

Radiofrequency ablation is a procedure done in the Catheterization Laboratory to help correct specific problems that cause the heart to beat faster than it should. Quality of life includes the physical as well as the emotional aspects of a patient. Doctors have always tried to take care of a medical problem with minimal physical and emotional risk. It is assumed that once the medical problem is fixed, the patient will have an improved quality of life. To know if this assumption is true, the investigators are asking children scheduled for this procedure, along with their family, to answer questions before the ablation, then answer the same questions 5-6 months after the ablation.

NCT ID: NCT00159185 Completed - Quality of Life Clinical Trials

Epidemiology Study in Major Orthopaedic Surgery

Start date: January 2004
Phase: N/A
Study type: Observational

The purpose of this study is to: - Create a database including a description of the patient population that undergoes total hip replacement with special emphasis on orthopedic and cardiovascular complications and the quality of life 1 year postoperatively. - Characterise the patient at risk for the above mentioned events - Create methods for predicting patients at risk for short-term (90 days) and long term (1 year) complications in relation to hip replacement surgery.