Clinical Trial: Time course changes of implant stability with FINESIA Relios system (Japan)

Tokyo, Nov. 13 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059751) titled 'Time course changes of implant stability with FINESIA Relios system' on Nov. 12. Study Type: Observational Primary Sponsor: Institute - Nagasaki University Condition: Condition - molar tooth loss Classification by malignancy - Others Genomic information - NO Objective: Narrative objectives1 - To measure the temporal changes of ISQ (Implant Stability Quotient) value o...


Clinical Trial: Effect of pemafibrate for hypertriglyceridemia with erectile dysfunction (Japan)

Tokyo, Nov. 13 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059746) titled 'Effect of pemafibrate for hypertriglyceridemia with erectile dysfunction' on Nov. 12. Study Type: Interventional Study Design: Basic Design - Single arm Randomization - Non-randomized Blinding - Open -no one is blinded Control - Uncontrolled Primary Sponsor: Institute - Showa Medical University Condition: Condition - Hypertriglyceridemia and Erectile Dysfunction Class...


Clinical Trial: Evaluation of the analgesic effect of adding intraoperative pulsed radiofrequency therapy to conventional perioperative pain management (Japan)

Tokyo, Nov. 13 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059742) titled 'Evaluation of the analgesic effect of adding intraoperative pulsed radiofrequency therapy to conventional perioperative pain management' on Nov. 12. Study Type: Interventional Study Design: Basic Design - Parallel Randomization - Non-randomized Blinding - Open -no one is blinded Control - No treatment Primary Sponsor: Institute - St. Luke's International University Co...


Clinical Trial: An observational study on treatments for postural abnormalities in Parkinson's disease and related disorders (Japan)

Tokyo, Nov. 13 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059747) titled 'An observational study on treatments for postural abnormalities in Parkinson's disease and related disorders' on Nov. 12. Study Type: Observational Primary Sponsor: Institute - National Research and Development Agency, NNational Center of Neurology and Psychiatry Condition: Condition - Parkinson's disease and related disorders Classification by malignancy - Others Geno...


Clinical Trial: To verify the analgesic effect of intraoperative pulsed radiofrequency therapy during thoracic surgery to alleviate postoperative pain (Japan)

Tokyo, Nov. 13 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059744) titled 'To verify the analgesic effect of intraoperative pulsed radiofrequency therapy during thoracic surgery to alleviate postoperative pain' on Nov. 12. Study Type: Interventional Study Design: Basic Design - Parallel Randomization - Non-randomized Blinding - Open -no one is blinded Control - No treatment Primary Sponsor: Institute - St. Lukes International University Cond...


Clinical Trial: An Exploratory Study on the Relationship Between Right Ventricular Isovolumic Relaxation Time, Pulmonary Vascular Load, and Clinical Outcomes in Patients with COPD (Japan)

Tokyo, Nov. 12 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059694) titled 'An Exploratory Study on the Relationship Between Right Ventricular Isovolumic Relaxation Time, Pulmonary Vascular Load, and Clinical Outcomes in Patients with COPD' on Nov. 12. Study Type: Observational Primary Sponsor: Institute - Nippon Medical School Hospital Condition: Condition - Chronic Obstructive Pulmonary Disease (COPD) Classification by malignancy - Others Ge...


Clinical Trial: A Before-and-After Study on the Impact of Switching from Conventional Icosapent Ethyl (EPA) Formulations to a Self-Emulsifying High-Purity EPA Formulation on Atherosclerotic Risk (Japan)

Tokyo, Nov. 12 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059728) titled 'A Before-and-After Study on the Impact of Switching from Conventional Icosapent Ethyl (EPA) Formulations to a Self-Emulsifying High-Purity EPA Formulation on Atherosclerotic Risk' on Nov. 12. Study Type: Interventional Study Design: Basic Design - Single arm Randomization - Non-randomized Blinding - Open -no one is blinded Control - Uncontrolled Primary Sponsor: Instit...


Clinical Trial: Examination of the Change in Quality of Life through an Environmental Sensor-Based Stress Estimation and Coping Feedback System for Healthy Individuals (Japan)

Tokyo, Nov. 11 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059590) titled 'Examination of the Change in Quality of Life through an Environmental Sensor-Based Stress Estimation and Coping Feedback System for Healthy Individuals' on Nov. 11. Study Type: Interventional Study Design: Basic Design - Single arm Randomization - Non-randomized Blinding - Open -no one is blinded Control - Uncontrolled Primary Sponsor: Institute - Graduate School of Me...


Clinical Trial: The exploratory study on the effect of peptide-containing foods in healthy adults: A randomized, double-blind, parallel-group controlled trial (Japan)

Tokyo, Nov. 11 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059724) titled 'The exploratory study on the effect of peptide-containing foods in healthy adults: A randomized, double-blind, parallel-group controlled trial' on Nov. 11. Study Type: Interventional Study Design: Basic Design - Parallel Randomization - Randomized Blinding - Double blind -all involved are blinded Control - Placebo Primary Sponsor: Institute - Faculty of Agriculture,Kyu...


Clinical Trial: A Phase III Clinical Study of CHO in Subjects with Ocular Discomfort (Japan)

Tokyo, Nov. 11 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059716) titled 'A Phase III Clinical Study of CHO in Subjects with Ocular Discomfort' on Nov. 11. Study Type: Interventional Study Design: Basic Design - Single arm Randomization - Non-randomized Blinding - Open -no one is blinded Control - Uncontrolled Primary Sponsor: Institute - ROHTO pharmaceutical CO.,LTD Condition: Condition - Subjects who have subjective symptoms of ocular dry...