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OpenTrials
Completed

NCT Number: NCT00551356

Lispro Mix 25 vs. Glargine in Type 2 Diabetics

In patients with type 2 diabetes who have not been on insulin therapy before the study will achieve better glycemic control by the treatment regiment consisting of two times daily insulin lispro mix 25 than by the treatment regiment with consisting of one time daily injection of insulin glargine. Improved glycemic control will be compared by the fasting plasma glucose and blood glucose excursions 2 hours after breakfast.

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Key information

Age range

30 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

Mexico City, Mexico

About this study

The objective of this study is to investigate which type of insulin regimen is the best way to achieve best glycemic control in early type 2 diabetes. Patients with diabetes mellitus type 2 with a duration of diabetes between 1 and 10 years without previous insulin therapy will be randomized on insulin lispro mix 25 or insulin glargine therapy. Glycemic control will be compared by the between treatment difference in fasting plasma glucose and 2h postprandial blood glucose excursions (preprandial -postprandial excursions) after breakfast.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Males or females who have type 2 diabetes between 1 and 10 years
  • Have used diet and/or maximum doses of oral antidiabetic agents (combination) for the treatment of their diabetes
  • Have not been on insulin treatment within 3 months before entry into the study
  • Have a hemoglobin A1c in the range of 8.0 to 12.5% according to a local laboratory within 4 weeks prior to or at Visit 1
  • Have a body mass index below 40 kg/m²

Exclusion criteria

  • Receive chronic (lasting longer than 2 weeks) systemic glucocorticoid therapy (excluding topical and inhaled preparations) or have received such therapy within 2 weeks immediately prior to Visit 1
  • Have a known allergy to insulin
  • Have serum creatinine greater than or equal to 1.5 mg/dl as determined by a local laboratory
  • Have known proliferative retinopathy
  • Have had more than one unexplained episode of severe hypoglycemia (defined as requiring assistance of another person due to disabling hypoglycemia) within 6 months prior to entering the study

Treatment and study plan

Insulin lispro mix 25

Drug

Insulin lispro mix 25 given SC twice-daily in conjunction with oral antidiabetic medications.

Other names: Humalog Mix25

Glargine

Drug

Insulin glargine given SC once-daily in conjunction with oral antidiabetic medications.

Other names: Lantus

Primary outcomes

  1. Change from baseline to endpoint in 2h postprandial blood glucose excursion after breakfast

    Time frame: 16 weeks or end of study.

Secondary outcomes

  1. Hemoglobin A1c measured at endpoint

    Time frame: 16 weeks or end of study.

  2. Change of hemoglobin A1c from baseline to endpoint

    Time frame: 16 weeks or end of study.

  3. Glycemic control as determined by self-monitored blood glucose concentrations

    Time frame: 16 weeks or end of study.

  4. The incidence and rate of self-reported hypoglycemic episodes

    Time frame: 16 weeks or end of study.

  5. Body mass index (BMI)

    Time frame: 16 weeks or end of study.

  6. Body weight

    Time frame: 16 weeks or end of study.

  7. Total Insulin Doses

    Time frame: 16 weeks or end of study.

Sponsors and collaborators

Lead sponsor

Eli Lilly and Company

Industry

Registry information

Official study title

Comparison of the Insulin Therapies: Insulin Lispro Low Mix (25%) and Insulin Glargine in Patients With Diabetes Mellitus Type 2

Acronym: IOOL

Important dates

Study start
2002
Study completion
2003
First posted
Oct 31, 2007
Registry last updated
Oct 31, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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