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Clinical Trials/JPRN-UMIN000001329
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

Kyoto Prefectural University of medicine0 sites60 target enrollmentAugust 21, 2008

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.

Registry
who.int
Start Date
August 21, 2008
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

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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