Clinical Trials Logo

Filter by:
NCT ID: NCT01998555 Active, not recruiting - Clinical trials for Coronary Artery Disease

Web-based Psychological Intervention to Coronary Artery Heart Disease Patients

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

The purpose of this study is to evaluate medical cost-effectiveness, reduce the psychological risk factors( including hostility, anxiety, depression, and perceived stress) in coronary artery disease (CAD) patients and enhance the regulation of the autonomic nervous system (including respiration rate, heart rate, distal blood vessel pulse, and finger temperament) through web-based cognitive -behavioral group therapy.

NCT ID: NCT01993992 Active, not recruiting - Anxiety Clinical Trials

Parental Anxiety and Its Relationship With Pediatric Patients' Post-operative Responses

Start date: December 2013
Phase: N/A
Study type: Observational

Post-operative delirium had multiple risk factors, such as pre-operative anxiety status, post-operative pain, and anesthetic method. We currently decrease pre-operative anxiety by parental accompanying until the children put to sleep. However, references indicate that parental anxiety can increase the post-operative delirium. Heart rate variability was used to measure the anxiety status of parents. We think sympathetic tone elevation measured by heart rate variability may not induce by anxiety alone, thus we want to explore this question by using Stat-Trait Anxiety Inventory questionnaire.

NCT ID: NCT01989988 Active, not recruiting - Clinical trials for Diabetes Mellitus Type 2 in Obese

DMBSS-A Randomized Trial of Different Laparoscopic Gastric Bypass Surgery in Patients With Obesity-related T2DM

DMBSS
Start date: January 2013
Phase: N/A
Study type: Interventional

The investigators would like to conduct a randomized clinical trial to compare the efficacy of diabetes treatment between different gastric bypass procedures involving type 2 diabetics patients with BMI from 27.5 to 35 kg/m2

NCT ID: NCT01967212 Active, not recruiting - Dysphagia Clinical Trials

Swallowing Training Combined With Game-based Biofeedback in Post-stroke Dysphagia

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

The purpose of this study is to determine whether swallowing training combined with game-based biofeedback is effective in the treatment of dysphagia due to stroke.

NCT ID: NCT01960595 Active, not recruiting - Pain Clinical Trials

Post-operative Pain Management In Patients Undergoing Hullax Valgus Surgery

Start date: August 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate the efficacy and cost analysis of intravenous fentanyl combined with either local anesthesia infiltration or peroneal nerves block in patients with Hallux Valgus undergoing orthopedic corrective surgery and compared with patients without local anesthetics administration perioperatively.

NCT ID: NCT01956409 Active, not recruiting - Clinical trials for Magnetic Resonance Imaging

Proton MR Spectroscopy and 18F-Fluorocholine PET for Breast Cancer Diagnosis

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

The application of FCH PET in breast cancer diagnosis has not been reported. We hypothesize that FCH reveals choline metabolic profiles of breast cancers, and shows the similar pathophysiological mechanism to choline on proton MRS, and our study goals are: 1. To investigate and compare the diagnostic performance of proton MRS and FCH PET for localized findings on mammography and breast ultrasound. 2. To investigate whether FCH PET findings are correlated with choline signals on proton MRS. 3. To evaluate if choline, water and lipid signals on proton MRS, FCH PET are associated with factors related to clinical outcome and prognosis- that is, molecular markers, tumor staging, histologic grade of breast cancers. 4. For localized advanced breast cancer, to investigate the treatment response to NAC using proton MRS and FCH PET, and to evaluate which modality is more sensitive. 5. To investigate the usefulness of FCH PET for whole body staging for breast cancer patients.

NCT ID: NCT01946204 Active, not recruiting - Prostatic Neoplasms Clinical Trials

A Study of Apalutamide (ARN-509) in Men With Non-Metastatic Castration-Resistant Prostate Cancer

SPARTAN
Start date: October 14, 2013
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of apalutamide in adult men with high-risk non-metastatic castration-resistant prostate cancer.

NCT ID: NCT01943097 Active, not recruiting - Neuroblastoma Clinical Trials

Evaluation of 18F-dopa and 123I-MIBG Uptake in the Patients With Neuroblastoma

Start date: June 2007
Phase: N/A
Study type: Observational [Patient Registry]

Neuroblastic tumors are childhood neoplasms that possess amino acid decarboxylase (AADC) activity and Meta-iodobenzylguanidine(MIBG), they can theoretically be imaged by (18)F-fluorodihydroxyphenylalanine ((18)F-FDOPA) and (123)I-Meta-iodobenzylguanidine((123)I-MIBG) PET, they are new and specific diagnostic and follow-up tools for neuroendocrine tumors. In this study, we explored the accuracy and clinical role of (18)F-FDOPA and (123)I-MIBG PET in neuroblastic tumors. METHODS: Patients with tissue-proven neuroblastic tumors receiving (18)F-FDOPA PET or (123)I-MIBG at initial diagnosis or during follow-ups were enrolled. The sensitivity and specificity of (18)F-FDOPA or (123)I-MIBG PET were compared to each other and compared to(18)F-FDG PET, using tumor histology as the standard.

NCT ID: NCT01926041 Active, not recruiting - Diabetes Mellitus Clinical Trials

The Effectiveness of Smoking Cessation in Prediabetic Smokers

Start date: August 1, 2013
Phase: N/A
Study type: Interventional

Existing literature investigating the impact of smoking cessation on new-onset diabetes mellitus (DM) risk is conflicting. Combing the need for smoking cessation and body weight self-management to prevent the progression of prediabetes stage into DM, with the public implementation of the second-generation cessation program, we aimed to study the effectiveness of the Fight Tobacco and Stay Fit (FIT2) program aiming at promoting smoking cessation and restricting post-cessation weight gain (PCWG) together in prediabetic smokers regarding long-term glycemic and DM-related health outcomes.

NCT ID: NCT01920568 Active, not recruiting - Fractures, Bone Clinical Trials

A Study to Compare Denosumab With Zoledronic Acid in Subjects With Bone Metastases From Solid Tumors

Start date: August 2013
Phase: Phase 3
Study type: Interventional

This is a randomized, double-blind, double-dummy study designed to provide bridging data in an Asian population to Amgen's studies of denosumab in subjects with bone metastases from solid tumors. The study is designed to provide data to a large global dataset of phase-III studies including breast cancer, prostate cancer, and all solid tumors, plus multiple myeloma, to support the regulatory approval for marketing and patient access to denosumab for the prevention of SREs in Chinese subjects with bone metastases from solid tumors. The primary objective of this study is to evaluate and compare the percent change from baseline to Week 13 in the bone marker urinary amino-terminal cross-linking telopeptide of type I collagen (uNTx) corrected for urine creatinine (uNTx/uCr) in subjects treated with denosumab to those treated with zoledronic acid. The study is designed to test the superiority of denosumab over zoledronic acid.