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Trial Comparing Insulin Detemir Morning, Insulin Detemir Evening and NPH Insulin Evening as Add-on to Oral Antidiabetic Drug(s) in Subjects with Type 2 Diabetes - Article


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Clinical Trial: Trial Comparing Insulin Detemir Morning, Insulin Detemir Evening and NPH Insulin Evening as Add-on to Oral Antidiabetic Drug(s) in Subjects with Type 2 Diabetes

This study is currently recruiting patients.

Sponsored by: Novo Nordisk
Information provided by: Novo Nordisk

Purpose

This trial will compare the use of insulin determir once a day to NPH insulin once a day when added to treatment with oral antidiabetic agents in patients with Type 2 diabetes. HbA1C results on each treatment will be measured and compared.

Condition Treatment or Intervention Phase
Diabetes Mellitus, Type II
 Drug: insulin detemir
 Drug: NPH (insulin)
Phase III

MedlinePlus related topics:  Diabetes

Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Parallel Assignment, Safety/Efficacy Study

Further Study Details: 
Primary Outcomes: HbA1C results
Expected Total Enrollment:  500

Study start: February 2005;  Expected completion: December 2005
Last follow-up: October 2005;  Data entry closure: November 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 and Contact Information

Novo Nordisk Clinical Trial Call Center      866-867-7178 

Alabama
      Calera,  Alabama,  35040,  United States; Recruiting

Arizona
      Phoenix,  Arizona,  85029,  United States; Recruiting

      Mesa,  Arizona,  85205,  United States; Recruiting

California
      Anaheim,  California,  92801,  United States; Recruiting

      Fullerton,  California,  92835,  United States; Recruiting

      San Diego,  California,  92128,  United States; Recruiting

      La Jolla,  California,  92037,  United States; Recruiting

Colorado
      Wheat Ridge,  Colorado,  80033,  United States; Recruiting

Massachusetts
      Waltham,  Massachusetts,  02453,  United States; Recruiting

      Fall River,  Massachusetts,  02721,  United States; Recruiting

Missouri
      Jefferson City,  Missouri,  65109,  United States; Recruiting

Nevada
      N. Las Vegas,  Nevada,  89030,  United States; Recruiting

New York
      New York,  New York,  10029,  United States; Recruiting

      Lewiston,  New York,  14092,  United States; Recruiting

      Williamsville,  New York,  14221,  United States; Recruiting

North Dakota
      Grand Forks,  North Dakota,  58201,  United States; Recruiting

Ohio
      Cincinnati,  Ohio,  45291,  United States; Recruiting

      Dayton,  Ohio,  45406,  United States; Recruiting

Pennsylvania
      Reading,  Pennsylvania,  19606,  United States; Recruiting

      Connellsville,  Pennsylvania,  15425,  United States; Recruiting

      Norristown,  Pennsylvania,  19401,  United States; Recruiting

South Carolina
      Greer,  South Carolina,  29651,  United States; Recruiting

Texas
      Conroe,  Texas,  77384,  United States; Recruiting

      Harker Heights,  Texas,  75648,  United States; Recruiting

Washington
      Seattle,  Washington,  98195,  United States; Recruiting

More Information

Study ID Numbers:  NN304-1632
Record last reviewed:  April 2005
Last Updated:  April 6, 2005
Record first received:  February 23, 2005
ClinicalTrials.gov Identifier:  NCT00104182
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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