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Completed Not applicable Interventional Results available

A Clinical Study to Evaluate the Use of Episodic, Intensive Blood Glucose Monitoring in Persons With Non-insulin Treated Type 2 Diabetes

ClinicalTrials.gov ID: NCT00674986

Public ClinicalTrials.gov record NCT00674986. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 9:44 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This randomized, parallel group study will determine whether the use of episodic, intensive glucose monitoring via the Accu-Chek 360 view blood glucose analysis system has a positive effect on overall glycemic control. Patients will be randomized into either the 'usual care' group, or the 'interventional group' supplemented with the Accu-Chek 360 view blood glucose analysis system. The effect of each treatment regimen on glycemic control will be assessed by measurement of change in baseline HbA1c values at 12 months. The anticipated time on study treatment is 1 year, and the target sample size is 504 individuals.

Study identification

NCT ID
NCT00674986
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
522 participants

Conditions and interventions

Eligibility (public fields only)

Age range
25 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 29, 2008
Primary completion
Jan 31, 2010
Completion
Jan 31, 2010
Last update posted
Oct 20, 2013

2008 – 2010

United States locations

U.S. sites
29
U.S. states
12
U.S. cities
25
Facility City State ZIP Site status
Not listed Mobile Alabama AL 36608
Not listed Pell City Alabama AL 35125
Not listed Chipley Florida 32428
Not listed Marianna Florida 32446
Not listed Pembroke Pines Florida FL 33028
Not listed Tampa Florida 33613
Not listed Tampa Florida 33624
Not listed Atlanta Georgia GA 30312
Not listed Atlanta Georgia GA 30342
Not listed Chicago Illinois 60616
Not listed O'Fallon Illinois IL 62269
Not listed Fishers Indiana IN 46038
Not listed Indianapolis Indiana 46256
Not listed Indianapolis Indiana In 46217
Not listed Flint Michigan 48504
Not listed Hickory North Carolina NC 28602
Not listed Raleigh North Carolina 27609
Not listed Wilmington North Carolina 28401
Not listed Winston-Salem North Carolina 27103
Not listed Cuyahoga Falls Ohio OH 44223
Not listed Zanesville Ohio OH 43701
Not listed Pottstown Pennsylvania 19468
Not listed Pottstown Pennsylvania PA 19464
Not listed High Point South Carolina SC 29720
Not listed Lancaster South Carolina SC 29720
Not listed Mt. Pleasant South Carolina 29464
Not listed Bristol Tennessee 37620
Not listed Crossville Tennessee TN 38555
Not listed Abingdon Virginia VA 24210

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00674986, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 20, 2013 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00674986 live on ClinicalTrials.gov.

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