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A Study to Evaluate the Blood Glucose Regulation and Safety of PPB-R-203-02 Based Noodle Versus Commercially Available Wet Noodle in Patients With Diabetes

2014-08-27 03:14:38 | BioPortfolio

Summary

To evaluate the result of PPB-R-203-02 based noodle and commercially available wet noodle on blood glucose control in 24 patients with diabetes for 2 days.

Description

The MiniMed Medtronic CGMS (continuous glucose monitoring system), the first model approved by FDA, was used for subcutaneous glucose monitoring. The CGMS continually measures the glucose concentration of the interstitial fluid every 10 seconds and then stores an average glucose value for each 5 minutes period, for a total of up to 288 measurements each day.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject), Primary Purpose: Health Services Research

Conditions

Diabetes Mellitus

Intervention

Commercially Available Wet Noodle, PPB-R-203-02 Noodle

Location

PingTung Christian Hospital
Pingtung
Taiwan

Status

Recruiting

Source

Pharma Power Biotec

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:14:38-0400

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