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NCT ID: NCT02774707 Enrolling by invitation - Dry Eye Syndrome Clinical Trials

Comparing the Quality of Topical Autologous Serum in Different Etiologies of Dry Eye Syndrome

Start date: January 2016
Phase: N/A
Study type: Observational

Human autologous serum is commonly used in the treatment of dry eye disease. However, different patients may have different effect with autologous serum treatment. We would like to find if different autologous serum had different component of cytokines in different etiologies of dry eye.

NCT ID: NCT02685839 Enrolling by invitation - Frailty Syndrome Clinical Trials

Development of an Intelligent POWER Rehabilitation Cluster Machine and Its Clinical Testing and Assessment

Start date: May 2015
Phase: N/A
Study type: Interventional

Elderly care has become one of the most important subjects in Taiwan and "frailty syndrome" are the most common problems among the elderly. In view of this trend, Taipei Veteran Memorial Hospital imported POWER rehabilitation from Japan in 2008. While showing significant clinical benefits, investigators have found that the system still has certain limitations (e.g. high cost, requires large space, patients must commute to the center, lacks real-time objective feedback , boring routines makes staying power to motivate patients for long term rehabilitation programs.) To overcome the above limitations, this project proposes an evidence-based rehabilitation model that accounts for actual clinical need and collaborates with our engineering team to develop a "cluster" , "wearable" and "Brain-Computer Interface System" version of POWER rehabilitation system. Combining cloud technology, investigators now introduce internet-of-things into the POWER rehabilitation procedure. The result will lower the burden of clinical support personnel, and provide an opportunity to quantify "frailty syndromes" so as to allow objective and quantitative scientific evaluation, leading to a more objective clinical diagnosis. In addition, this project further proposes a virtual-reality (VR) system for POWER rehabilitation, as well as designs for the VR sceneries. Through the use of different animated 3D VR sceneries and interactive game design, investigators can make rehabilitation interesting and fun for the patients, motivating long-term compliance of the patients, thereby, improving the clinical outcome of POWER rehabilitation. This project has the potential to create an innovative solution to address the current bottlenecks of our rehabilitation treatment model. Successful development of the system will offer rehabilitation clinicians more treatment options, lower the cost of supporting staff, reduce commuting cost for the patients, and elevate patient desire to comply with the treatment program. Finally, the system will not only enhance Taiwan's academic reputation in the international arena, it will also generate new commercial opportunities for Taiwan and contribute to Taiwan economic development.

NCT ID: NCT02648776 Enrolling by invitation - Sleep Disorders Clinical Trials

Risk and Benefit Assessment of Hypnotic Agents for Sleep Disorders Among Elderly

RABA-HASDE
Start date: January 2016
Phase: Phase 4
Study type: Observational

The aims of this study are to (1) examine the medication use patterns of commonly prescribed hypnotics and the factors that were associated with the long-term and short-term use patterns among the elderly population in Taiwan; (2)investigate the associations of using hypnotics with the elderly patients' disease statuses, efficacy and safety, as well as its pharmacokinetic and pharmacogenetic characteristics;(3) determine the clinical, economic and humanistic outcomes of using hypnotics and the corresponding contributing factors for the elderly in Taiwan.

NCT ID: NCT02644317 Enrolling by invitation - Development Delay Clinical Trials

The Balance Influence of Shoe Inserts on Motor Development Delayed Children

Start date: December 2015
Phase: N/A
Study type: Interventional

Flatfoot, one of the most common foot problems experienced by preschool-aged children, characterized by the collapse of the foot's medial longitudinal arch. Children with motor developmental delay often have flatfoot, according to clinical observation, and research indicates that preschool age is the main stage of the medial longitudinal arch development period. There flatfoot symptoms due to poor arch shock effect, poor walking endurance, likely to cause gait problems while growing up. The lack of a stable foot structure to support and maintain posture may lead to delayed motor development. Early training intervention and help to balance stability is the main rehabilitation goal for motor developmental delayed children. With understanding of the foot development of motor development delayed children, proper intervention can be provided to improve the movement and stability of the lower limbs. The possible deformation of the foot structure and resultant pain in the future can also be prevented.

NCT ID: NCT02616575 Enrolling by invitation - Clinical trials for Peer Review, Health Care

The Application of Smart Health Management System on Home-Care for Elderly Patients

Start date: December 2015
Phase:
Study type: Observational

Aims: The purposes of this study are 1. to create a smart living environment with home care system using GPS and cloud-based services for elderly people. 2. to improve the home care system from user feedback and recommendations. Methods: Participants (n = 50) will be recruited from geriatric clinics in National Taiwan University Hospital (NTUH) main hospital and its Beihu branch. Enrollment criteria include: aged 60 or older, living alone or with one companion (not children), taking at least one chronic medications, having the capability to understand the study and complete the study, willing to participate into the study with telephone follow ups.

NCT ID: NCT02556073 Enrolling by invitation - Asthma Clinical Trials

ICS/LABA Combination With Integrated Dose Counter and Smartphone APP to Improve Asthma Control

Start date: August 2014
Phase: N/A
Study type: Interventional

Poor adherence to asthma controller medication may link to poor asthma outcome. A metered dose device with built-in dose counter helps physicians to monitor drug compliance in asthma patients. Mobile-phone based self management opens a window for better asthma control. The present study aims to investigate the relationship between the adherence to controller medication of combined inhaled corticosteroid/long acting beta2-agonists, assessing by integrated dose counter, and the level of airway inflammation and asthma control. Moreover, the investigators also use a new asthma self-management Apps to enhance drug compliance. With the application of the new, easily available tools, the investigator expect to increase adherence rates, and hence, to reduce airway inflammation and improve the level of asthma control.

NCT ID: NCT02422628 Enrolling by invitation - Lung Cancer Clinical Trials

Correlation Between EGFR Mutation Using cfDNAs and Circulating Tumor Cells in Patients With NSCLC

Start date: April 2015
Phase: N/A
Study type: Observational

Correlation of epithelial growth factor receptor mutation in blood of lung cancer patient and clinical outcome.

NCT ID: NCT02311036 Enrolling by invitation - Clinical trials for Cerebrovascular Diseases

Functional Recovery Effects on Comprehensive Rehabilitation for Post-acute Care -Cerebrovascular Diseases

Start date: December 2014
Phase: N/A
Study type: Interventional

The purpose of the study is to investigate the effects and outcome predictors on functional recovery after comprehensive rehabilitation for post-acute care -cerebrovascular diseases.

NCT ID: NCT02289365 Enrolling by invitation - Radiodermatitis Clinical Trials

Orally Administrated JBM-TC4 Prevents Acute Radiodermatitis in Breast Cancer Patients

Start date: November 2014
Phase: Phase 2
Study type: Interventional

This trial is designed as a multicenter, double-blinded, randomized, placebo controlled study to assess the safety and efficacy of JBM-TC4 for the prevention and treatment of acute radiation-induced dermatitis in breast cancer patients receiving radiotherapy.

NCT ID: NCT02276235 Enrolling by invitation - Obese Women Clinical Trials

The Therapeutic Effect of Catgut Embedding in Obesity

Start date: January 2014
Phase: Phase 4
Study type: Interventional

The aim of this double-blind, randomized, placebo-controlled trial is to evaluate the therapeutic effects of acupoint stimulation by catgut embedding on complexion, quality of life, lipid profile, inflammatory markers, and obesity-related hormone peptide of obese women.