Clinical Trial: A study to evaluate the effect of the food containing peptides intake on serum uric acid (Japan)

Tokyo, Oct. 1 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000058823) titled 'A study to evaluate the effect of the food containing peptides intake on serum uric acid' on Oct. 1. Study Type: Interventional Study Design: Basic Design - Parallel Randomization - Randomized Blinding - Double blind -all involved are blinded Control - Placebo Primary Sponsor: Institute - HUMA R&D CORP Condition: Condition - None Classification by malignancy - Others G...


Clinical Trial: Reexamination of the correlation between caffeine concentrations in blood and saliva (Japan)

Tokyo, Oct. 1 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059186) titled 'Reexamination of the correlation between caffeine concentrations in blood and saliva' on Oct. 1. Study Type: Interventional Study Design: Basic Design - Single arm Randomization - Non-randomized Blinding - Open -no one is blinded Control - Uncontrolled Primary Sponsor: Institute - Department of Pharmacology, Graduate School of Medicine, Ehime University Condition: Cond...


Clinical Trial: Comparison of recovery profile after remimazolam-fentanyl anesthesia and propofol-fentanyl anesthesia for pulsed field ablation: a prospective randomized trial (Japan)

Tokyo, Oct. 1 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059210) titled 'Comparison of recovery profile after remimazolam-fentanyl anesthesia and propofol-fentanyl anesthesia for pulsed field ablation' on Oct. 1. Study Type: Interventional Study Design: Basic Design - Parallel Randomization - Randomized Blinding - Single blind -participants are blinded Control - Active Primary Sponsor: Institute - Hiroshima Heart Center Condition: Condition...


Clinical Trial: An Interventional Study on Nurses' Napping During Night Shifts:Comparison of Sleep Efficiency Before and After the Introduction of Reclining Beds (Japan)

Tokyo, Oct. 1 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000058811) titled 'An Interventional Study on Nurses' Napping During Night Shifts:Comparison of Sleep Efficiency Before and After the Introduction of Reclining Beds' on Oct. 1. Study Type: Interventional Study Design: Basic Design - Single arm Randomization - Non-randomized Blinding - Open -no one is blinded Control - Uncontrolled Primary Sponsor: Institute - Kobe University Condition: C...


Clinical Trial: Exploration of parametersin blood correlated with saticfaction after consumption of animal based foods or plantbased foods (Japan)

Tokyo, Oct. 1 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000057219) titled 'Exploration of parametersin blood correlated with saticfaction after consumption of animal based foods or plantbased foods' on Oct. 1. Study Type: Interventional Study Design: Basic Design - Cross-over Randomization - Randomized Blinding - Double blind -all involved are blinded Control - Placebo Primary Sponsor: Institute - Fuji Oil Holdings Inc. Condition: Condition -...


Clinical Trial: Cohort study of gingival recession utilizing an intraoral scanner and root caries (Japan)

Tokyo, Oct. 1 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059157) titled 'Prospective study of gingival recession utilizing an intraoral scanner and root caries' on Oct. 1. Study Type: Observational Primary Sponsor: Institute - Sunstar Inc. Condition: Condition - Gingival recession, Root caries Classification by malignancy - Others Genomic information - NO Objective: Narrative objectives1 - Characterize the extent and location of gingival re...


Clinical Trial: Measurement of Auditory Evoked Responses in Children Using gASSR (Japan)

Tokyo, Oct. 1 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000058938) titled 'Measurement of Pediatric Auditory Evoked Responses' on Oct. 1. Study Type: Observational Primary Sponsor: Institute - International University of Health and Welfare Condition: Condition - hearing loss Classification by malignancy - Others Genomic information - NO Objective: Narrative objectives1 - In previous studies, we measured gap-evoked auditory steady-state respon...


Clinical Trial: Mandibular Reconstruction with Custom Made Titanium Mesh Tray and PCBM Harvested from Ilium and Tibia: A Clinical Study (Japan)

Tokyo, Oct. 1 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059013) titled 'Clinical Evaluation of Mandibular Reconstruction Using Titanium Mesh Tray and Particulate Cancellous Bone and Marrow from Ilium and Tibia' on Oct. 1. Study Type: Interventional Study Design: Basic Design - Single arm Randomization - Non-randomized Blinding - Open -no one is blinded Control - Uncontrolled Primary Sponsor: Institute - Tsurumi University Condition: Condit...


Clinical Trial: Elucidating the association between the etiology of pediatric acute appendicitis and oral Fusobacterium (Japan)

Tokyo, Oct. 1 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059106) titled 'The relationship between pediatric acute appendicitis and periodontal bacteria' on Oct. 1. Study Type: Observational Primary Sponsor: Institute - University of Tsukuba Condition: Condition - Aute appendicitis Classification by malignancy - Others Genomic information - NO Objective: Narrative objectives1 - Elucidating the etiology of pediatric acute appendicitis Basic o...


Clinical Trial: Effects of daily consumption of dried finely powdered asparagus on the reduction of eye and nasal discomfort for 8 weeks: A randomized, double-blind, placebo-controlled parallel-group comparison study (Japan)

Tokyo, Oct. 1 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059055) titled 'Effects of daily consumption of dried finely powdered asparagus on the reduction of eye and nasal discomfort for 8 weeks: A randomized, double-blind, placebo-controlled parallel-group comparison study' on Oct. 1. Study Type: Interventional Study Design: Basic Design - Parallel Randomization - Randomized Blinding - Double blind -all involved are blinded Control - Placebo ...