A exploratory study for the effects of antioxidant form of coenzyme Q10 (ubiquinol)

UMIN ID: UMIN000019107

Registered date:24/09/2015

Basic Information

• Recruitment status: Complete: follow-up complete
• Health condition(s) or Problem(s) studied: Subjects with tendency of constipation or diarrhea
• Date of first enrollment: 2015/10/01
• Target sample size: 50
• Countries of recruitment: Japan
• Study type: Interventional

Intervention(s)

antioxidant form of coenzyme Q10 (Ubiquinol) 50mg 3 capsuls (150mg) 1 time a day A group for 24 weeks, B group for 12 weeks
placebo capsule 3 capsuls1 time a day B group for 12 weeks

Outcome(s)

• Primary Outcome: 1)The change of defecation and fecal form 2)QOL 3)Cognitive function These are evaluate in baseline, 12 weeks, and 24 weeks after intervention

Key inclusion & exclusion criteria

• Age minimum: 60years-old
• Age maximum: Not applicable
• Gender: Male and Female
• Exclude criteria: 1) Patients who have allergic to test food 1) Patients who have serious complications 2) Pregnant 3) Others

Related Information

• Primary Sponsor: Yuri-Kumiai General Hospital
• Source(s) of Monetary Support: KANEKA Coporation