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Quality of Life clinical trials

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NCT ID: NCT01855009 Recruiting - Quality of Life Clinical Trials

Study of Parental Ratings of Quality of Life and Body Composition in 5-19 Year Olds While Participating in the Good NEWS 4 Kids Program

Start date: May 2013
Phase: N/A
Study type: Interventional

This study will compare changes in body composition (lean mass, fat, and bone)and parent ratings of quality of life in 5-19 Year Olds as a function of participation in one of four versions of the Good NEWS 4 Kids Program (GN4K).

NCT ID: NCT01850095 Recruiting - Quality of Life Clinical Trials

The Influence of Peripheral Androgen Conversion at Women Adult Acne

Start date: March 2012
Phase: N/A
Study type: Interventional

Acne vulgaris is a chronic inflammatory disease that affects the pilosebaceous unit. Recent studies have demonstrated an increase number of acne cases in adult women. These cases are predominantly normoandrogenic and have some clinical differences when compared with the most common group, the adolescent. The local glandular metabolism converts some hormonal precursors to more active substances that increase the sebum production, leaving these areas more prone to increase the colonization to Propionibacterium Acnes (P. Acnes). Toll-like receptor 2, expressed by inflammatory cells play a crucial role in the innate immune response to this bacterium. Previous studies confirm that exist a reduced expression of CD1d by keratinocytes in acne lesion, what can be interpreted as a low antigen-present function. The influence of hormonal alteration in the sebaceous glands could modulate the expressions of TLR-2 and CD1d explaining the persistence of lesions in adult women. The change to more estrogenic metabolism, with use of specific contraceptive pills could normalize this immune-mediated inflammatory process. Objective To analyze how the peripheral androgen conversion can influence the toll-like receptor 2 and CD1d expression in women with inflammatory acne before and after 6 months of oral contraceptives with anti-androgen activity.

NCT ID: NCT01848223 Recruiting - Quality of Life Clinical Trials

The Quality of Life in Late Menopause

QoL
Start date: November 2012
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the quality of life of late postmenopausal Finnish women and the factors affecting it.

NCT ID: NCT01747642 Recruiting - Quality of Life Clinical Trials

Safety and Efficacy of Oncoxin Plus Surafineb in Hepatocellular Carcinoma

Start date: December 2012
Phase: Phase 2/Phase 3
Study type: Interventional

Oncoxin in combination with Surafenib is safe and results in improved survival in patients with hepatocellular carcinoma (HCC)

NCT ID: NCT01734122 Recruiting - Parkinson Disease Clinical Trials

Stereotactic Radiosurgery for Essential Tremor and Parkinsonian Tremor

Start date: February 21, 2013
Phase:
Study type: Observational

The purpose of this study is to determine the changes in quality of life and degree of tremor for patients with essential tremor or Parkinsonian tremor who are treated by stereotactic radiosurgery (SRS). This is a questionnaire-based study. Please see Detailed Description below for more information.

NCT ID: NCT01664013 Recruiting - Quality of Life Clinical Trials

The Impact of Botulinum Toxin Treatment in Quality of Life of Cervical Dystonia Patients

Start date: October 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate the impact of botulinum toxin treatment in quality of life(QoL) in cervical dystonia patients

NCT ID: NCT01657487 Recruiting - Quality of Life Clinical Trials

Comparing Treatment Efficacy With High and Medium Dose of Fluticasone in Combination With Salmeterol in COPD Patients

Start date: April 2010
Phase: Phase 4
Study type: Interventional

This study is to investigate and compare treatment efficacy with high and medium dose of fluticasone in combination with salmeterol in COPD patients.

NCT ID: NCT01638741 Recruiting - Depression Clinical Trials

The Need for Rehabilitation and the Connection With Attachment Styles Among Patients With Gynaecological Cancer

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

The purpose of this study is to provide new knowledge about: - Integration of rehabilitation in a highly specialized gynaecological department. - Development and testing of an individually adapted rehabilitation process. - Needs for rehabilitation among women with gynaecological cancer. - Connection between adult attachment style for women with gynaecological cancer and their quality of life, rehabilitation needs and symptoms of depression /PTSD.

NCT ID: NCT01587976 Recruiting - Quality of Life Clinical Trials

Health Related Quality of Life After Surgery and Oncological Treatment of Colorectal Liver Metastases

HQOL
Start date: June 2011
Phase: N/A
Study type: Observational

The purpose of this trial is to study health related quality of life (HQoL)after resection of colorectal liver metastases combined with perioperative chemotherapy. The investigators want to study if an aggressive, life prolonging and multimodal treatment can be defended from a quality of life perspective.

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.