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An Observational Study Evaluating Efficacy, Safety and Convenience of NovoNorm® in Treatment of Type 2 Diabetes in Routine Clinical Practice

NCT ID: NCT01498900

Last Updated: 2016-10-28

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

Total Enrollment

30554 participants

Study Classification

OBSERVATIONAL

Study Start Date

2004-08-31

Study Completion Date

2006-07-31

Brief Summary

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This study is conducted in Africa and Asia. The aim of this study is to evaluate the efficacy, safety and convenience of using repaglinide (NovoNorm®) in type 2 diabetes management in routine clinical practice.

Detailed Description

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Conditions

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Diabetes Diabetes Mellitus, Type 2

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Repaglinide

repaglinide

Intervention Type DRUG

Prescription according to the product labelling at the physicians' discretion

Interventions

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repaglinide

Prescription according to the product labelling at the physicians' discretion

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Type 2 diabetes
* Newly diagnosed or not adequately controlled with current therapy
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Novo Nordisk A/S

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Global Clinical Registry (GCR, 1452)

Role: STUDY_DIRECTOR

Novo Nordisk A/S

Locations

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Novo Nordisk Investigational Site

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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China Iraq Jordan Lebanon Morocco Turkey (Türkiye)

Related Links

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http://novonordisk-trials.com

Clinical Trials at Novo Nordisk

Other Identifiers

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AGEE-1875

Identifier Type: -

Identifier Source: org_study_id