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Trial record 6 of 36 for:    "Hyperglycemia" | "Insulin Aspart"

Effects of Insulin Treatment on Postprandial Platelet Activation in Patients With Non-insulin-dependent Diabetes Mellitus (NIDDM)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00771693
Recruitment Status : Completed
First Posted : October 13, 2008
Last Update Posted : November 5, 2010
Information provided by:
Karolinska Institutet

Brief Summary:

The postprandial phase in diabetic patients is characterized by a rapid increase in blood glucose levels, increase in platelet aggregation, LDL oxidation and over production of thrombin.

The aim of the study is to determine whether meal induced platelet activation is related to post-prandial hyperglycemia, and can be attenuated by good postprandial glucose control with rapidly acting insulin in patients with T2DM.

Condition or disease Intervention/treatment Phase
Type 2 Diabetes Mellitus Postprandial Hyperglycemia Drug: Insulin aspart (Novorapid®) Phase 4

Detailed Description:

Each patient is admitted in the fasting state, on 3 different occasions . Blood glucose levels are normalized using intravenous infusion of insulin aspart , to a blood glucose level of 6-7 mmol/l. 15 minutes after normalization ,and right before a standardized meal, the patient is given a subcutaneous injection of insulin aspart 0.1 U/kg, 0.2 U/kg or placebo. The order of injections in the cross over study is randomized and blinded to the patient and to the investigators. The patient eats the meal and is followed up for 90 minutes after completion of the meal.

Blood tests for platelet function and other parameters are taken at 3 main points: 1. before glucose normalization.

2. 15 minutes after glucose normalization, and right before the meal. 3. 90 minutes after the meal.

Platelet function is evaluated by flow cytometry in whole blood (P- Selectin expression, Fibrinogen binding,aggregate formation: platelet- leukocyte, platelet-platelet, platelet-monocyte). Agonists that are used for platelet activation in flow cytometry are the thromboxane analogue U46619, ADP, and a collagen peptide that activates GPVI. Platelet adhesion is measured by the IMPACT cone and platelet analyser.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 18 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Basic Science
Official Title: Effects of Insulin Treatment on Postprandial Platelet Activation in Patients With NIDDM: a Placebo-controlled Dose-response Study With Insulin Aspart (Novorapid®)
Study Start Date : May 2007
Actual Primary Completion Date : August 2010
Actual Study Completion Date : August 2010

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Hyperglycemia

Intervention Details:
  • Drug: Insulin aspart (Novorapid®)
    a cross-over study with subcutaneous injection of insulin aspart 0.1U/kg, 0.2u/kg or placebo, before the meal, on 3 different occasions.
    Other Name: NovoRapid (Novo-Nordisk)

Primary Outcome Measures :
  1. To evaluate if platelet activation following a carbohydrate rich meal is related to the post-prandial hyperglycemia, and thus can be attenuated by premeal insulin treatment in patients with T2DM. [ Time Frame: 90 minutes after the meal ]
  2. Co- primary platelet response variables: U46619 stimulated platelet P- selectin activation, platelet-leukocyte aggregation, platelet-platelet aggregates and platelet-monocyte aggregates. [ Time Frame: After completion of the study in 20 patients ]

Secondary Outcome Measures :
  1. To elucidate if short-term lowering of blood glucose by insulin infusion (pretreatment standardization of blood glucose) reduces platelet activity in patients with T2DM. [ Time Frame: After completion of the glucose normalization (before the meal) ]

Information from the National Library of Medicine

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Ages Eligible for Study:   up to 70 Years   (Child, Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Type II Diabetes Mellitus.
  • Antecubital forearm veins allowing technically good sampling for platelet studies.
  • HbA1c 6-9 % (Mono-S method).
  • Below 70 years

Exclusion Criteria:

  • History of a cardiovascular disease; Ischemic heart disease, Stroke, Peripheral vascular disease.
  • Acute or chronic renal or liver disease
  • Contraindication to insulin treatment
  • Treatment with Glitazones, Sulphonylurea, antiplatelet drugs,
  • Thrombocytopenia <150 X109/l.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00771693

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Department of Medicine, Clinical pharmacology Unit, Karolinska University Hospital, Solna.
Stockholm, Sweden, SE 171 76
Sponsors and Collaborators
Karolinska Institutet
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Principal Investigator: Paul Hjemdahl, MD, PhD Department of Medicine, Clinical Pharmacology Unit, Karolinska institute, Stockhom, Sweden

Publications automatically indexed to this study by Identifier (NCT Number):
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Responsible Party: Prof. Paul Hjemdahl, Dept Medicine Solna, Clinical Pharmacology Unit, Karolinska Institute, Stockholm, Sweden Identifier: NCT00771693     History of Changes
Other Study ID Numbers: EudraCT number 2006-007031-27
First Posted: October 13, 2008    Key Record Dates
Last Update Posted: November 5, 2010
Last Verified: November 2010
Keywords provided by Karolinska Institutet:
Platelet Activation
Postprandial hyperglycemia
Additional relevant MeSH terms:
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Insulin Aspart
Insulin degludec, insulin aspart drug combination
Diabetes Mellitus
Glucose Metabolism Disorders
Metabolic Diseases
Endocrine System Diseases
Insulin, Globin Zinc
Insulin, Long-Acting
Hypoglycemic Agents
Physiological Effects of Drugs