JPRN-UMIN000001329
Completed
Phase 2
A Randomized trial to assess the effects of hydrogen-rich dissolution water for patients with impaired glucose tolerance or impaired fasting glucose
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Kyoto Prefectural University of medicine
- Enrollment
- 60
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\) Patients who are abele to give written informed consent
- •2\) FBS is over 100mg/dl and under 126mg/dl in registration
- •3\) Age is over 20 years and less than 80 years
- •4\) Type of practice: outpatient department
- •5\) Patients are able to do the following things in this trial \- getting good compliance with consuming investigational food and coming to hospital, and writing the diary and the questionnaire accurately by themselves
Exclusion Criteria
- •1\) Patients who have receive drug treatment for diabetes
- •2\) Patients with the diseases which have possibility with impaired glucose tolerance
- •3\) Patients with serious liver or kidney damage
- •4\) Patients with serious heart disease or cerebrovascular disorders
- •5\) Patients with serious disease in pancreas or blood disease
- •6\) Patients with malignant tumors which effect their general status or survival time
- •7\) Patients who are in pregnancy, while breast\-feeding, have possibilities of them, or desire pregnancy in test period
- •8\) Patients with alcohol abuse
- •9\) Patients who have taken part in the her clinical research within 12 weeks
- •10\) Patients who have taken part in the her clinical research within 12 weeks
Outcomes
Primary Outcomes
Not specified
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