Approved Study Database
| Ref. No. | Scientific Title | Principal investigator |
|---|---|---|
| 2006.400 | A 54-Week, Double-Blind, Randomized, Placebo-Controlled, Parallel-Group Study to Investigate the Effects of Rosiglitazone (Extended Release Tablets) as Adjunctive Therapy to Acetycholinesterase Inhibitors on Cognition and Overall Clinical Response in APOEe4-Stratified Subjects with Mild to Moderate Alzheimer's Disease (REFLECT-3) | Prof. Mok CT. Vincent |
| 2009.145 | A 52-Week, 2-Period, Multicenter, Randomized, Double-Blind, Donepezil-Referenced, Placebo-Controlled, Efficacy, and Safety Study of 3 Dosage Levels of SAM-531 in Outpatients With Mild to Moderate Alzheimer Disease | Prof. Kwok Chi Yui, Timothy |
| 2013.213 | A 52-week treatment, multi-center, randomized, double-blind, double dummy, parallel-group, active controlled study to compare the effect of QVA149 (indacaterol maleate / glycopyrronium bromide) with salmeterol/fluticasone on the rate of exacerbations in subjects with moderate to very severe COPD | Prof. HUI David Shu Cheong |
| 2004.183 | A 52-Week Randomized, Double-blind, Parallel-Group, Multi-Centre, Active-Controlled (Glibenclamide) Study to Evaluate the Efficacy, Safety and Tolerability of Tesaglitazar Therapy when Administered to Patients with Type 2 Diabetes | Prof. Chan C.N. Juliana |
| 2007.381 | A 52-week Open-label Extension Study of the Long-term Safety and Efficacy of Rosiglitazone Extended-release (RSG XR) as Adjunctive Therapy to Acetylcholinesterase Inhibitors in Subjects with Mild-to-moderate Alzheimer | Prof. Mok C.T. Vincent |
| 2002.051 | A 52-Week Multicentre Randomized Double-Blind Double Dummy Placebo-Controlled Parallel Group Study to Compare the Efficacy and Tolerability of Salmeterol/Fluticasone 50/100Mmcg Once Daily in the Morning - - - Asthmatic Subjects | Prof. Wong Wing Kin Gary |
| 2009.262 | A 52 week randomized, controlled, open label, multicentre, multinational treat-to-target trial comparing efficacy and safety of SIBA and insulin glargine both administered once daily in a basal-bolus regimen with insulin aspart as mealtime insulin | Prof Wu Justin, Che-yuen |
| 2011.597 | A 52 week Randomised, Double-blind, Placebo-controlled Study to Investigate the Efficacy and Safety of GSK1605786A in the Maintenance of Remission in Subjects with Crohn's Disease | Dr Ng Siew Chien |
| 2011.604 | A 5-year study to compare the durability of glycemic control of a combination regimen with vildagliptin & metformin versus standard-of-care monotherapy with metformin, initiated in treatment-naïve patients with type 2 diabetes mellitus | Dr. OZAKI Risa |
| 2011.605 | A 5-year study to compare the durability of glycemic control of a combination regimen with vildagliptin & metformin versus standard-of-care monotherapy with metformin, initiated in treatment-naïve patients with type 2 diabetes mellitus | Dr. TSANG Chiu Chi |
| 2018.244 | A 5-year follow-up study of psychological functions of non-demented community dwelling older adults in Hong Kong. |
Dr. XIONG Shing Chuen 熊丞荃 |
| 2013.568 | A 48 weeks, phase II, randomized, double-blind, placebo-controlled, proof of concept and dose finding study of three different dose regimens of BI 655066 administered subcutaneously in patients with ankylosing spondylitis. | Prof. TAM Lai Shan |
| 2015.110 | A 40-year-old question – what is the functional receptor for human norovirus? |
Dr. CHAN Martin Chi Wai 陳子蔚 |
| 2017.636 | A 3D Software and Bone Quality Assessment Validation of Low Dose Biplanar X-ray EOS Imaging System based on Retrospective Collected Imaging Data |
Prof. CHENG Jack Chun Yiu 鄭振耀 |
| 2009.017 | A 3-Year, Multicenter, Double-blind, Randomized, Placebo-Controlled Extension to CZOL446H2301E1 to Evaluate the Efficacy and Long Term Safety of 6 and 9 Years Zoledronic Acid Treatment of Postmenopausal women with Osteoporosis | Prof. Leung Ping Chung |
| 2006.025 | A 3-year, Double-blind Extension to CZOL446H2301 to Evaluate the Long Term Safety and Efficacy of Zoledronic Acid in the Treatment of Osteoporosis in Postmenopausal Women Taking Calcium and Vitamin D | Prof. Leung Ping Chung |
| 2019.258 | A 3-year prospective study of offspring of patients with bipolar disorder: determining emergence of mood disorder and predictive value of circadian rhythm disturbance | Dr. ZHANG Jihui |
| 2006.221 | A 3-month Epidemiological Study to Establish Characteristics of Asian Patients with Acute Major Depressive Disorder | Prof. Wing Yun Kwok |
| 2017.336 | A 3 year longitudinal study of the level of asthma control and treatment of asthma patients in Hong Kong |
Dr. CHAN Ka Pang 陳嘉鵬 |
| 2016.058 | A 2D-3D Modeling Scheme for 3D Lung Reconstruction Derived from Low Dose Biplanar X-ray in Standing Position- with Clinical Validation in Adolescent Idiopathic Scoliosis |
Prof. CHU Winnie Chiu Wing 朱昭穎 |
| 2005.063 | A 26 Week, Double-blind, Randomized, Multicenter, Parallel Group, Active-controlled Study Comparing Aliskiren to Ramipril with Optional Addition of Hydrochlorothiazide, Followed by a 4 Week Double-blind, Randomized, Placebo-Controlled Withdrawal in Patients with Essential Hypertension | Prof. Yu Cheuk Man |
| 2015.370 | A 24-week, multinational, multicentre, randomised, open label, parallel-group treat to target trial to compare efficacy and safety of thrice daily versus twice daily NovoMix®30 (Biphasic insulin aspart 30) in subjects with type 2 diabetes inadequately controlled with basal insulin |
Dr. CHOW Francis Chun Chung 周振中 |
| 2010.347 | A 24-week, multi-center, double-blind, randomized, placebo-controlled, parallel-group study to assess the efficacy and safety of vildagliptin 50mg bid as an add-on therapy to insulin, with or without metformin, in patients with type 2 diabetes mellitus | Dr. Risa Ozaki |
| 2005.022 | A 24-week Randomized, Double-Blind, Parallel-Group, Multi-Centre, Active-Controlled (Metformin or Metformin Combined with Fenofibrate) Study to Evaluate the Lipid Metabolic Effects, Safety and Tolerability of Tesaglitazar Therapy in Patients with Type 2 Diabetes and Low HDL-Cholesterol on a Fixed Background Therapy with a Statin | Prof. Kong PS Alice |
| 2004.182 | A 24-Week Randomized, Double-blind, Double-dummy, Multicenter Study to Compare the Efficacy of Extended Release AVANDIA_ (8mg OD) and Immediate-Release AVANDIA (8mg OD) in Subjects with Type 2 Diabetes Mellitus | Prof. Chan C.N. Juliana |
| 2019.451 | A 24-week multi-center, double-blind, placebo controlled dose-range finding study to investigate the efficacy and safety of oral QBW251 in COPD patients on triple inhaled therapy (LABA/LAMA/ICS) |
Prof. HUI David Shu Cheong 許樹昌 |
| 2003.263 | A 24 Weeks, Multi-Centre, Randomized, 2-Arm Parallel, Open-Labelled Study to Investigate the Efficacy and Safety of Initiating Biphasic Insulin Aspart 30 (BIAsp 30) in Type 2 Diabetes Patients Currently Not Achieving Treatment Targets with Oral Anti-Diabetes Drugs Alone (BIAsp-3021, Phase IV) | Dr. Chow Chun Chung Francis |
| 2022.492 | A 20-year follow-up study of clinical, functional and neuro-biological outcomes first-episode schizophrenia spectrum and bipolar affective disorders. |
Dr. WONG Yip Chau 黃業就 |
| 2005.257 | A 2-Year Study to Assess the Efficacy, Safety, and Tolerability of Taranabant in Obese Patients Followed by a 1-Year Extension | Dr. Chow Chun Chung Francis |
| 2011.309 | A 2-year Observational Study on Eyelid Bags in Chinese: Analysis on anatomical components and progression | Professor Lam Dennis Shun Chiu |
| 2013.069 | A 2-Part, Phase 2/3 Study to Assess the Safety, Tolerability and Efficacy of AMG 145 in Subjects With Homozygous Familial Hypercholesterolemia Part A - Open-label, Single-arm, Multicenter Pilot Study to Evaluate Safety, Tolerability, and Efficacy of AMG 145 in Subjects With Homozygous Familial Hypercholesterolemia Part B - Double-blind, Randomized, Placebo-controlled, Multicenter Study to Evaluate Safety, Tolerability and Efficacy of AMG 145 in Subjects With Homozygous Familial Hypercholesterolemia | Professor Tomlinson Brian |
| 2008.153 | A 2 year extension to: A 76-week, Worldwide, Multicenter, Double-Blind, Randomized, Placebo-Controlled Study to Assess the Tolerability and Efficacy of Anacetrapib When Added to Ongoing Therapy with a Statin in Patients with Coronary Heart Disease (CHD) or CHD Risk-Equivalent Disease: Reversal period extended from 12 weeks to 1-year | Professor Tomlinson Brian |
| 2009.234 | A 17-Week, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multi-Center Trial Of Pregabalin For The Treatment Of Chronic Central Neuropathic Pain After Spinal Cord Injury | Associate Consultant Law Sheung Wai |
| 2007.138 | A 16 Week Open-Label Outpatient, Randomized, Parallel Study Assessing the Impact of Two Different Initial Dose Prescriptions for Dry Powder Inhaled Insulin (EXUBERA_) on Glycemic Control in Patients with Type 2 Diabetes Mellitus Who are Poorly Controlled on A Combination of Two or More Oral Agents | Prof. Tong C.Y. Peter |
| 2012.281 | A 14 week, randomized, double-blind, multi-center, parallel group, active controlled study to evaluate the efficacy and safety of LCZ696 in comparison to olmesartan in elderly patients with essential hypertension | Prof. Tomlinson Brian |
| 2006.233 | A 13-Week, Randomized, Multi-Center, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy, Safety and Tolerability of Pregabalin (150-600 MG/DAY) Using A Flexible Dosing Schedule in the Treatment of Subjects with Central Post-Stroke Pain (CPSP) | Prof. Wong Ka Sing Lawrence |
| 2020.101 | A 120-months review of the autopsy rate and discordant rates in a university-affiliated teaching hospital in Hong Kong | Dr. CHAN Ronald Cheong Kin |
| 2009.147 | A 12-year followup study of bone changes in Chinese women - the Hong Kong Perimenopausal women osteoporosis study | Prof. Ho (Chan) Suzaanne Sutying |
| 2007.427 | A 12-week, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter, Dose-Finding Study to Evaluate the Efficacy, Tolerability and Safety of Fesoterodine in Comparison to Placebo in Patients with Overactive Bladder | Dr PANG Selina |
| 2002.284 | A 12-week, Randomized, Double-blind, Parallel-group, Multicentre, Phase III Study to Compare the Efficacy and Safety of Symbicort ® pMDI (Budesonide/Formoterol 80/4.5ug 2 Actuations b.I.d., Delivered Dose) with that of Pulmicort ® pMDI (Budesonide100ug 2 Actuations b.I.d., Metered Dose) and Symbicort Turbuhaler ® (Budesonide/Formoterol 80/4.5 ug 2 Inhalations b.I.d., Delivered Dose) in Children with Asthma | Prof. Wong Wing Kin Gary |
| 2005.139 | A 12-week, Double-Blind, Randomized Study to Investigate the Effect of 500_g Roflumilast Tablets Once Daily Versus Placebo on Pulmonary Function in Patients with Chronic Obstructive Pulmonary Disease | Prof. Hui Shu Cheong David |
| 2008.416 | A 12-week Treatment, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Assess the Efficacy, Safety and Tolerability of Indacaterol (150 and 300 ug o.d.) in Patients with Chronic Obstructive Pulmonary Disease (COPD) | Prof. Hui Shu Cheong |
| 2017.611 | A 12-week randomized, patient and investigator blinded, placebo-controlled, parallel group study to investigate the efficacy of LIK066 in obese patients with non-alcoholic steatohepatitis (NASH) |
Prof. WONG Vincent Wai Sun 黃煒燊 |
| 2011.026 | A 10-year outcome study of an early intervention program for psychosis in Hong Kong (EASY) compare with standard care service | Dr Chung Wai Sau |
| 2015.698 | A 10-year Naturalistic Follow-up Study of Insomnia in Major Depressive Disorder - Focusing on Clinical and Neuropsychological Outcomes |
Prof. WING Yun Kwok 榮潤國 |
| 2013.011 | A 10-year follow-up study on obstructive sleep apnoea in a population-based cohort: a cardiovascular perspective | Prof Li Albert Martin |
| 2024.169 | A 10-year Cluster Based Retrospective Cohort Study of Patients with AQP4-IgG Positive Neuromyelitis Optica Spectrum Disorder (NMOSD) in Hong Kong | Dr. CHOI Chun Ho Joseph |
| 2019.366 | A 'Sweet Dream - Sugar Down' (SD-SD) programme to promote sleep and better glycaemic control in patients with type 2 diabetes mellitus. |
Ms. NGAN Hau Yi 顏巧尔 |
| 2016.011 | 7-year Follow-up of the Jockey Club Early Psychosis (JCEP) Project Early Intervention Trial for First-episode Psychosis |
Dr. CHUNG Dicky WS 鍾維壽醫生 |
| 2007.296 | 5-Year Stability of ICD-10 Psychiatric Diagnoses in Patients Presented with First Episode Psychosis to the EASY (Early Assessment Service for Young People with Psychosis) Program in HKSAR | CHANG Wing Chung |
Page 252 of 254.