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DiabetesNCT01014832

Efficacy and Safety of Frequently Modified Intensive Insulin

A study testing Intensive insulin therapy in people with Diabetes, run by Hygieia, Inc at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to evaluate the efficacy and safety of frequently modified intensive insulin therapy in patients with Type-2 and Type-1 diabetes mellitus. Read more about this study

Who is it for?
Ages 25 to 65 years
Conditions the study is for
Diabetes
What is being tested?
Intensive insulin therapy
Could I receive a placebo?
No, everyone receives an active treatment
How many people
14 participants
Where
1 siteUnited States
Study dates
Dec 2008to Aug 2009
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 25 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Individuals eligible for inclusion in the study are those who:
  • are male or female, 25 to 65 years of age;
  • are of any ethnic background;
  • meet the criteria for either population I or population II;
  • if a female of child-bearing potential will submit to a urine pregnancy test (UPT) at Visit 1;
  • can provide their previous 12 months of lab results (at least one set of blood count, kidney functions, and liver enzymes); and
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  • read, understand, and sign an informed consent document which contains a Health Information Portability and Accountability Act (HIPAA) authorization after being advised of the nature of the study.
  • Population I inclusion criteria:
  • Individuals eligible for inclusion in population I are those who:
  • meet the standard criteria for enrollment in the study;
  • have been clinically diagnosed compatible with Type-2 diabetes for at least 1 year;
  • take insulin injections for the past 6 months;
  • have or have not been using an oral agent within the past 6 months;
  • have sufficient medical insurance coverage to cover intensive insulin therapy including Lantus® and Humalog®/Novolog® as well as test-strips cost for testing their blood glucose levels at least 4 times per day;
  • are willing to stop anti-diabetic agents (except Metformin);
  • are willing to accept intensive insulin therapy with at least 4 daily insulin injections;
  • consistently record their glucose measurements and insulin doses in a log book and have their previous readings ready for review; and
  • have a Hemoglobin-A1c (HbA1c) of 7.6% or greater, to be drawn at Visit 1.
  • Population II inclusion criteria:
  • Individuals eligible for inclusion in population II are those who:
  • meet the standard criteria for enrollment in the study;
  • have been clinically diagnosed compatible with Type-1 diabetes for at least 1 year;
  • treated with both long acting insulin analog (ie, Insulin Glargine) and short acting insulin analog (ie, Insulin Lispro or Insulin Aspart) with a total daily insulin dose of 25 units or more
  • are currently using carbohydrate counting in their regimen or have been trained to employ this technique during the last 2 years;
  • consistently record their glucose measurements and insulin doses in a log book and have their previous readings for review; and
  • have a HbA1c of 7.6% or greater, to be drawn at Visit 1.

Who cannot join

  • Individuals excluded from participation in the study are those who:
  • have a history of greater than 2 episodes of severe hypoglycemia (See Section 5.4) in the past year or hypoglycemic unawareness;
  • have a significant physical, psychological, or cognitive impairment that would prohibit adherence to an intensive insulin therapy program;
  • have any severe cardiovascular disease including a history of congestive heart failure (New York Heart Association [NYHA] 3 or 4), unstable angina, myocardial infarction or stroke that occurred within 6 months prior to enrollment
  • have a history of severe anemia with a hematocrit less than 25% in women or 30% in men;
  • have a history of renal disease (ie, serum creatinine level greater than 2.0 mg/dl);
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  • have a history of active cancer or cancer in the past 2 years (except non-melanoma skin cancer);
  • are receiving chemotherapy or radiation therapy;
  • have a history of significant liver disease including cirrhosis or elevated liver function tests (AST and ALT) greater than 3 times the upper limit of normal values;
  • have a body mass index (BMI) greater than 45 kg/m2; and/or
  • are pregnant, plan to become pregnant during the study period, or are breastfeeding.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • TKL Research INC.

    Paramus, New Jersey, 07652

Other trials in United States

About this study

Official title: An Efficacy and Safety Evaluation of Frequently Modified Intensive Insulin Therapy in Subjects With Uncontrolled Type-I or Type-2 Diabetes

The purpose of this study is to evaluate the efficacy and safety of frequently modified intensive insulin therapy in patients with Type-2 and Type-1 diabetes mellitus.

Read the detailed description

Insulin treatment is the mainstay of Type-1 diabetic management and one of the cornerstones in Type-2 diabetes. This treatment is based on multiple daily injections of different types of insulin. Patients follow their endocrinologists' directions by adhering to a set of recommended dosages and formulas, calculated by repeated blood glucose measurements. In order to maintain effective and safe management, glucose measurements are taken before meals and at bedtime, albeit imposing a heavy financial burden on a patient and their support system. For illustration, each disposable glucosemeter strip costs more than a dollar and needs to be replaced routinely 4 times daily, yielding an annual cost of more than $1500 per patient. Insulin dosages necessitate repeated adjustments to meet the patient's changing needs. Variations in food intake, body weight, physical activity, on going medical conditions and mood can impact a patient's insulin needs.

Accordingly, at each diabetic clinic appointment, the endocrinologist reviews the patient's glucose measurements and insulin doses to determine whether the insulin dosage needs to be adjusted. Unfortunately, limited appointment availability restricts insulin dosages adjustments to once every several months. Furthermore, as a result of the limited time allotted for each patient, new dosing recommendations are based on a review of only the most recent measurements. This drawback may be one of the chief causes of suboptimal management, with merely 38% of diabetic patients able to achieve proper control and mitigate detrimental complications.

Since the discovery of insulin by Frederick Grant Banting in 1921, only stringent glucose control by a regimen of multiple insulin injections has prevented microvascular and macrovascular complications in Type 1 diabetic patients. Moreover, insulin treatment amongst other treatment modalities has been shown to prevent microvascular and macrovascular complications in Type-2 diabetic patients. Incidentally, as the Type-2 diabetic epidemic expands, insulin treatment is becoming one of the main treatment modalities. Not taking into consideration availability, it has been established that more frequent patient-clinic interactions improve diabetic management in both Type-1 and Type-2 patients.

In a typical 3-6 month interval appointment, the endocrinologist would measure a patient's hemoglobin A1c (HbA1c) to determine the quality of the last 3 months control. This value, is linearly correlated to mean glucose levels at that 3 months period and, therefore, can be predicted according to the measurements. We used anonymous records of glucose measurements to perform preliminary statistical analysis. Our results indicate that a patient's glucose level is a highly non-stationary process, with strong variations in both mean and standard deviation (SD) from one week to another. In many patients with excessive HbA1c, which are at levels that diabetic complications are likely to ensue, the endocrinologist is obligated to adjust the insulin dosage based on a review of the patient's most recent glucose values and the values of the past several weeks. Furthermore, since appointment timing is random and independent from the patient's measurements, random trends in glucose values may be identified that lead to different conclusions. For illustration, if a patient's appointment happens to occur when his glucose values randomly trend up, the endocrinologist may choose to increase insulin doses. On the other hand, if the appointment occurs at a time when the glucose levels trend down, he may act oppositely. The required frequency of follow-up and dose adjustment that yields better patient control is yet to be determined.

Studies have shown that case management in patients with Type-2 diabetes can allow better control of HbA1c levels. These studies have involved using qualified medical professionals (ie, nurses, pharmacists, physician's assistants) as intervention methods, as well as providing counseling and follow-up calls to help patients with improved self-management of diabetes.

This study is designed to show that weekly insulin dosage adjustments for intensive insulin therapy are superior to conservative, infrequent adjustments during clinical appointments in both Type-1 and Type-2 diabetes.

Conditions
Diabetes
Being tested
Intensive insulin therapy
Keywords
Diabetes, insulin.
Medical subject headings
Diabetes Mellitus, Insulin Resistance

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Intensive insulin therapyDrug

    Also called Basal-bolus insulin therapy

    Intensive insulin therapy

Study groups in NCT01014832
Study groupRoleWhat they receive
Uncontrolled diabetesExperimentalUncontrolled diabetes
Receives: Drug: Intensive insulin therapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Hemoglobin A1C

    Measured: 12 weeks

  2. Mean weekly glucose

    Measured: 12 weeks

  3. Frequency of hypoglycemia

    Measured: 12 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Nov 2009 (estimated)
  2. Study startDec 2008
  3. Primary completionAug 2009
  4. Study completionAug 2009

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
14 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01014832
Sponsor's protocol ID
Hygieia study -2
Other IDs
CS950308
Status last verified
Nov 2009
First submitted
13 Nov 2009
Last updated
17 Nov 2009
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A study testing Intensive insulin therapy in people with Diabetes, run by Hygieia, Inc at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 26 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 17 Nov 2009. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Hemoglobin A1C (time frame: 12 weeks). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Nov 2009; AzTrials last refreshed its copy on 7 Nov 2026.

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