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Quality of Life clinical trials

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NCT ID: NCT01654900 Not yet recruiting - Quality of Life Clinical Trials

Mid-term Survival and Quality of Life of Elderly Patients Undergoing Open Heart Surgery

Start date: October 2012
Phase: N/A
Study type: Observational

The purposes of the investigators study is to examine the overall survival and quality of life in elderly patients (> 75 years) undergoing open heart surgery at Hadassah medical center between 2008-2011. All alive patients will be phone interviewed using the 36-item short form health survey. Results will be compared to similar health survey results (36-SF)obtained from a group of Israeli adults who had no open heart surgery (controlled group). The investigators hypothesize that elderly patients achieve improvement in quality of life after open heart surgery with acceptable operative morbidity and mortality.

NCT ID: NCT01608997 Not yet recruiting - Quality of Life Clinical Trials

Postoperative Multiparameter Outcomes During the Six Months After Rotator Cuff Repair

Start date: June 2012
Phase: N/A
Study type: Observational

Rotator cuff tears are common amongst 50-60 year olds with no connection to their physical activity. When symptomatic, the injury affects all aspects of general health, quality of life and function. Surgical intervention is recommended only if conservative treatment fails. The purpose of the surgical intervention is to reduce pain, and improve function while improving range of motion and muscle strength around the shoulder. The purpose of the current study is to measure physical, functional, expectation, satisfaction and quality of life outcomes after rotator cuff repair surgery. Another purpose is to learn the reproducibility components of the above outcomes.

NCT ID: NCT01475773 Not yet recruiting - Quality of Life Clinical Trials

Psychological Assessment of Adults Seeking Orthodontic Treatment

Start date: November 2011
Phase: N/A
Study type: Observational

Is their a association between the objective and subjective severity of a malocclusion, quality of life and self-esteem/personality (as modifier between objective/subjective severity and quality of life (cfr study Agou et al., 2008) ? A second goal is to compare motivation and expectations and the objective and subjective severity of the malocclusion on the other hand.

NCT ID: NCT01202812 Not yet recruiting - Quality of Life Clinical Trials

A Randomized Trial of LOVAZA in Pediatric Sickle Cell Disease (SCD)

Start date: October 2010
Phase: Phase 2
Study type: Interventional

The purpose of the study is to determine the effectiveness of LOVAZA (fish oil capsules) to decrease inflammation in children and adolescents with Sickle Cell Disease (SCD). It has been found that besides the damage caused by sickle red blood cells themselves, the inflammatory response that occurs in SCD patients could potentially play a significant role in the occurrence of painful episodes or pain crises. The investigators will also study whether the subject/caregiver feels that there is an improvement in the child's quality of life by taking the medication. Besides the effect of LOVAZA on inflammation,the investigators are also testing whether the drug will have a beneficial effect on blood clotting ability (which is known to be increased in SCD) and on the anemia (low red blood cells) that is part of the disease entity.

NCT ID: NCT01173952 Not yet recruiting - Quality of Life Clinical Trials

Quality of Life in Men Undergoing Robotic Assisted Laparoscopic Radical Prostatectomy Versus Radical Retropubic Prostatectomy

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

This study is prospective evaluation of quality of life in men undergoing robotic assisted laparoscopic radical prostatectomy versus radical retropubic prostatectomy.

NCT ID: NCT00457210 Not yet recruiting - Quality of Life Clinical Trials

The Influence of Radiotherapy on Cognitive Function

Start date: April 2007
Phase: N/A
Study type: Observational

The cognitive function of 150 patients that undergone any Radiotherapy treatment to the brain will be assessed at 3 time points before and after the treatment.