Insulin Glargine Vs Standard Insulin Therapy

Cystic Fibrosis Related Diabetes Clinical Trial

Official title:

Comparison of Insulin Glargine Vs Standard Insulin Therapy in CFRD Without Fasting Hyperglycemia

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00222521
• Other study ID #: 0205M25461
• Status: Completed
• Phase: Phase 3
• First received: September 14, 2005
• Last updated: September 14, 2005
• Start date: April 2003
• Est. completion date: August 2005

Study information

• Verified date: September 2005
• Source: University of Minnesota - Clinical and Translational Science Institute
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

This Study is designed to determine whether treatment of CFRD with glargine insulin will improve hemoglobin A1c, weight and muscle mass compared to the traditional regimen of bedtime NPH insulin.

Description:

The majority of cystic fibrosis (CF) patients now survive beyond childhood, and CF related diabetes (CFRD), due to insulin deficiency, is common. CFRD with fasting hyperglycemia occurs in about 15% of adult CF patients. Standard insulin therapy has relied primarily on meal coverage with rapid-acting insulin. Usually, basal insulin coverage is only provided overnight, with modest doses of NPH insulin. The practice of providing minimal basal insulin in CFRD is based on the fact that most of these patients, unless they are acutely ill, are able to maintain relatively normal blood glucose levels during the day without it. In addition, anecdotal experience has suggested that daytime NPH insulin or once to twice daily ultralente insulin frequently lead to hypoglycemia in the CFRD patient. This practice, which is based on practical clinical considerations, ignores the established relationship between insulin deficiency and clinical deterioration in CFRD. BMI and pulmonary function deteriorate much more rapidly in CF patients with diabetes than in CF patients with normal glucose tolerance. Insulin deficiency leads to increased protein catabolism and fatty acid turnover. The resulting loss of weight and lean body mass contributes to pulmonary disease and clinical decline.

We hypothesize that:

1. Basal insulin coverage with insulin glargine will improve hemoglobin A1c, weight, and muscle mass in patients with CFRD with fasting hyperglycemia, compared to traditional regimens with less basal insulin.

2. Because of the peakless action of insulin glargine, this will be accomplished without serious hypoglycemia.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: August 2005
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 12 Years and older

Eligibility

1. Inclusion Criteria

1. CFRD with fasting hyperglycemia (fasting plasma glucose =126 mg/dl)

1. . The diagnosis must be made at a time when the patient is in his/her basal state of health with no evidence of acute exacerbation in the preceding two months.

a). Acute exacerbation is defined on page 9.

2. . For patients with onset of diabetes in the preceding 6 months, the hemoglobin A1c must be stable for 3 months prior to study entrance within 5% (0.3% A1c increment).

2. Age =18, post-pubertal (done growing, since change in weight is a study endpoint)

3. Weight stable within 5% during the previous 3 months as measured in CF clinic

4. Willingness to attend all study visits and to engage in regular phone or e-mail contact with the study diabetes nurse

5. Glucocorticoids can have a profound effect on weight, and thus we wish to minimize the occurrence of changing steroid doses during the study period. Patients receiving glucocorticoid therapy will be included in the protocol only if:

1. . They have been on the same steroid dose for the preceding six months,

2. . There are no plans to change their steroid dose in the next eight months.

2. Exclusion Criteria

1. Pregnancy or plans to become pregnant in the next eight months (because of the changes pregnancy would cause in our study endpoints),

2. Unwillingness / inability to take multiple injections or to count carbohydrates,

3. A history of hypoglycemia unawareness (rare in CF),

4. Plans to start any medication in the next 8 months that might affect weight, such as testosterone or Megace. Patients chronically taking these medications may be included if:

1. . They have been on the same dose for the preceding six months

2. . There are no plans to change their dose in the next eight months

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Cystic Fibrosis
• Cystic Fibrosis Related Diabetes

Intervention

Drug:
• Glargine insulin

Locations

Country	Name	City	State
United States	University of Minnesota	Minneapolis	Minnesota

Sponsors (3)

Lead Sponsor	Collaborator
University of Minnesota - Clinical and Translational Science Institute	Moran, Antoinette, M.D., Sanofi

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Hemoglobin A1c
Secondary	BMI
Secondary	Body composition by DEXA Scan
Secondary	# Episodes of illness
Secondary	Quality of life survey