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Quality of Life clinical trials

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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: NCT01173861 Completed - Breast Cancer Clinical Trials

Effectiveness of a Cancer Center Based Physical Activity Intervention

Start date: March 2010
Phase: N/A
Study type: Interventional

Purpose: Examine the effectiveness of cancer center-based physical activity counseling on physical activity rates and quality of life in breast cancer survivors. Hypothesis: Participants in the intervention group will indicate greater step counts and quality of life at the end of the intervention compared to the control group

NCT ID: NCT01167855 Completed - Asthma Clinical Trials

Reducing Asthma Disparities Through School-Based Telemedicine for Rural Children

Start date: May 25, 2011
Phase: N/A
Study type: Interventional

The overall goal of this proposal is to examine the efficacy of a school-based asthma telemedicine intervention in a predominately minority, low-income rural pediatric population.

NCT ID: NCT01155011 Completed - Quality of Life Clinical Trials

Multilevel Intervention for Physical Activity in Retirement Communities

MIPARC
Start date: January 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to assess whether a 6-month multilevel physical activity intervention can significantly increase physical activity levels in sedentary adults, 65 and older, living in Continuing Care Retirement Communities (CCRCs). Sedentary residents (N=320)in 16 CCRCs will receive the multilevel MIPARC intervention or a control health education program for 6 months. A group randomized control design will be employed with site as the unit of randomization. The intervention is delivered through group sessions, phone calls, printed materials, tailored signage and mapping and targeted peer led advocacy efforts.

NCT ID: NCT01140659 Completed - Quality of Life Clinical Trials

Objective Evaluation of Patients With Palmar Hyperhidrosis Submitted to Two Levels of Sympathectomy: T3 and T4.

Start date: February 2007
Phase: N/A
Study type: Interventional

Compare the results obtained with video-assisted sympathectomy performed in two distinct levels ganglionic (third versus fourth thoracic ganglion) for the treatment of palmar hyperhidrosis, through a blind randomized clinical trial using an objective method to measure the sweat before and after the operation.

NCT ID: NCT01139749 Recruiting - Quality of Life Clinical Trials

Efficacy and Safety of Low-dose Oral Isotretinoin for Seborrhea

Start date: October 2011
Phase: Phase 4
Study type: Interventional

Oral isotretinoin is the gold standard drug to treat moderate to severe acne. Other indications like seborrhea, seborrheic dermatitis have been suggested. There is risk of reversible mucocutaneous side effects, as well as alterations in lipid profile and transaminases. The major problem is teratogenicity which demands pregnancy control from treatment beginning to one month after treatment end. Seborrhea and seborrheic dermatitis are chronic conditions characterized by oily skin, hair and scalp, erythema, desquamation and negative impact on quality of life. This will be an interventional, therapeutic and quality of life randomized, comparative (parallel groups), blinded evaluation clinical trial, comprising 50 men and women, aged 18 to 40. Treatment with low-dose oral isotretinoin will be compared to topical anti-seborrheic products to evaluate the reduction of sebaceous secretion and colonization of affected areas by yeasts of Malassezia gender. Efficacy will be evaluated by clinical parameters, as well as by sebum secretion measure and application of quality of life questionnaires. Safety will be evaluated by skin hydration measure, side effects report and observation. For subjects using oral isotretinoin blood counting, transaminases, lipid profile and pregnancy test will be requested as selection criteria, on days 30 and 180. Data will be submitted to statistical analysis.

NCT ID: NCT01132209 Completed - Pain Clinical Trials

Suture Techniques to Reduce the Incidence of The inCisional Hernia

STITCH
Start date: October 2009
Phase: N/A
Study type: Interventional

The objective of the study is reduction of the incidence of the most frequent complication of abdominal surgery, incisional hernia. In this multi center double-blinded prospective randomized controlled trial, in which a new suture technique using small bites is compared with the traditionally applied large bites (mass closure) technique for midline incisions.

NCT ID: NCT01127828 Completed - Quality of Life Clinical Trials

Effects of Cultura Yoghurt in Irritable Bowel Syndrome (IBS) Patients on Intestinal and Immunological Changes

Start date: September 2005
Phase: N/A
Study type: Interventional

To determine the effect of cultura probiotic yoghurt on number of responders to treatment during 8 weeks of treatment in comparison to placebo. To determine the effect of cultura yoghurt on change in total score of (IBS) irritable bowel syndrome severity index during 8 weeks of treatment in comparison to placebo in IBS out patients.

NCT ID: NCT01101711 Completed - Quality of Life Clinical Trials

Endocrine Dysfunction and Quality of Life After Subarachnoid Hemorrhage

Start date: November 2006
Phase: N/A
Study type: Observational

Investigation of the incidence of endocrine dysfunction following subarachnoid hemorrhage (SAH), and to see if this has a relation to CNS lesions as evaluated by MRI and to common symptoms after SAH such as general exhaustion, lack of initiative, increased sleep demand and reduced quality of life.

NCT ID: NCT01080547 Completed - Quality of Life Clinical Trials

Study Comparing Conventional and Fast Track Multi-Discipline Treatment Interventions for Colorectal Cancer

Start date: March 2010
Phase: Phase 3
Study type: Interventional

A new notion"Fast Track Multi-Discipline Treatment" for colorectal cancer is thought with several benefits such as shorter hospitalization stay and less costs. This randomized study aims to compare the differences between conventional and Fast Track Multi-Discipline Treatment for colorectal cancer in hospitalization day, complications, costs and quality of life.