AST Clinical Investigation

Overview

Blood glucose monitoring system are tested in the alternative site to validate the accuracy of the blood glucose.

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Parallel Assignment
    • Primary Purpose: Diagnostic
    • Masking: None (Open Label)
  • Study Primary Completion Date: December 2010

Interventions

  • Device: blood glucose monitor
    • Blood glucose monitor is used to monitor the blood glucose level of the human-being
  • Device: blood glucose monitor
    • Blood glucose monitor is used to monitor the blood glucose level of the human-being.

Arms, Groups and Cohorts

  • Experimental: Andon
    • Andon blood glucose test strips with test meter
  • Active Comparator: Lifescan

Clinical Trial Outcome Measures

Primary Measures

  • blood glucose value
    • Time Frame: 5 seconds

Participating in This Clinical Trial

Inclusion Criteria

  • people ( disbetes people)with at least 8 hours of limosis

Exclusion Criteria

  • After meal(when doing the test)
  • take Hypoglycemic Drugs(when doing the test)
  • with insulin(when doing the test)
  • after strenuous exercise(when doing the test)
  • Pregnant women
  • neonates
  • patients in a hyperglycemic-hyperosmolur state, with or without ketosis.
  • patients who are dehydrated, hypertensive, hypotensive or in shock.

Gender Eligibility: All

Minimum Age: 21 Years

Maximum Age: 78 Years

Are Healthy Volunteers Accepted: Accepts Healthy Volunteers

Investigator Details

  • Lead Sponsor
    • Andon Medical Co.,Ltd
  • Provider of Information About this Clinical Study
    • Yi Liu, Andon Medical Co.,Ltd

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