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Insulin Detemir plus Insulin Aspart vs. Insulin Glargine plus Insulin Aspart as Mealtime Insulin in Type II Diabetes - Article


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Insulin glargine

insulin glargine [rDNA origin]; Lantus



Clinical Trial: Insulin Detemir plus Insulin Aspart vs. Insulin Glargine plus Insulin Aspart as Mealtime Insulin in Type II Diabetes

This study is no longer recruiting patients.

Sponsored by: Novo Nordisk
Information provided by: Novo Nordisk

Purpose

The purpose of this study is to test whether insulin detemir is a safe and at least as effective alternative to insulin glargine for the control of blood glucose in basal/bolus therapy in patients with type II diabetes.

Condition Treatment or Intervention Phase
Diabetes Mellitus, Type II
 Drug: insulin detemir
 Drug: Lantus (insulin glargine)
 Drug: Novolog (insulin aspart)
Phase III

MedlinePlus related topics:  Diabetes

Study Type: Interventional
Study Design: Treatment, Safety/Efficacy Study

Further Study Details: 

Expected Total Enrollment:  300

Study start: September 2004;  Study completion: January 2006
Last follow-up: October 2005;  Data entry closure: December 2005

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both

Criteria

  • Type II diabetics age 18 or older that have had diabetes for at least 12 months.

Location Information


Arkansas
      Little Rock,  Arkansas,  72204,  United States

California
      Spring Valley,  California,  91978,  United States

      San Francisco,  California,  94143,  United States

      Inglewood,  California,  90301,  United States

      Santa Ana,  California,  92705,  United States

Florida
      Orlando,  Florida,  32804,  United States

      Melbourne,  Florida,  32901,  United States

      New Port Richey,  Florida,  34652,  United States

      Vero Beach,  Florida,  32960,  United States

      Boca Raton,  Florida,  33433,  United States

      Winter Park,  Florida,  32789,  United States

      Jacksonville,  Florida,  32205,  United States

Georgia
      Athens,  Georgia,  30606,  United States

Idaho
      Idaho Falls,  Idaho,  83404,  United States

Kansas
      Topeka,  Kansas,  66606,  United States

Nebraska
      Omaha,  Nebraska,  68131,  United States

Nevada
      Las Vegas,  Nevada,  89119,  United States

New Jersey
      Berlin,  New Jersey,  08009,  United States

North Carolina
      Asheville,  North Carolina,  28801,  United States

Pennsylvania
      Hermitage,  Pennsylvania,  16148,  United States

      Philadelphia,  Pennsylvania,  19107,  United States

Texas
      Dallas,  Texas,  75235,  United States

      Dallas,  Texas,  75246,  United States

      Dallas,  Texas,  75390-8858,  United States

      San Antonio,  Texas,  78229,  United States

Virginia
      Norfolk,  Virginia,  23502,  United States

      Richmond,  Virginia,  23249,  United States

Washington
      Tacoma,  Washington,  98405,  United States

More Information

Study ID Numbers:  NN304-1431
Record last reviewed:  March 2005
Last Updated:  March 18, 2005
Record first received:  November 17, 2004
ClinicalTrials.gov Identifier:  NCT00097084
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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November 18, 2008



Page Updated: September 6, 2005
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