Continuous Glucose Monitoring System (CGMS) in Type 2 Diabetic Patients Inadequately Controlled by Metformine Monotherapy; Analyze of Glycemic Profile Before and After Association of Glimepiride

NCT ID: NCT00633425

Last Updated: 2008-03-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

43 participants

Study Classification

INTERVENTIONAL

Study Start Date

2002-10-31

Study Completion Date

2003-10-31

Brief Summary

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Analyse the glucose profile, based on continuous glucose monitoring by CGMS, in type 2 diabetics inadequately controlled by metformin, before and after the addition of Glimepiride.

Detailed Description

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Conditions

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Diabetes Mellitus

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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GLIMEPIRIDE

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Men or women aged 35 to 70 years
* Having given their consent
* Type 2 diabetics (HBA1c greater than 6.5%
* Fasting glycaemia greater than 1.40 g/l) not controlled by Metformin for at least 6 weeks.
Minimum Eligible Age

35 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Sanofi

INDUSTRY

Sponsor Role lead

Principal Investigators

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Nathalie Billon

Role: STUDY_DIRECTOR

Sanofi

Locations

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Sanofi-Aventis

Paris, , France

Site Status

Countries

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France

Other Identifiers

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HOE490B_4001

Identifier Type: -

Identifier Source: org_study_id