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Comparison of the Management of Post-prandial Hyperglycemia by Multiple Bolus Calculators

NCT01050868 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2016-03-03

No results posted yet for this study

Summary

This prospective, non-randomized, non-controlled, interventional study will determine whether the Roche automated bolus caclulator (ABC) reduces post-meal hyperglycemia better than the competitor's ABC without causing significant hypoglycemia.

Conditions

  • Diabetes Mellitus Type 1

Interventions

DEVICE

Accu-Chek Combo Kit mg DE/de

Sponsors & Collaborators

Principal Investigators

  • Bettina Petersen · Roche Diagnostics GmbH / Diabetes Care

Study Design

Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-06-30
Primary Completion
2009-12-31
Completion
2009-12-31

Countries

  • Germany

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01050868 on ClinicalTrials.gov