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Effects of Insulin Detemir and NPH Insulin on Renal Handling of Sodium, Fluid Retention, and Weight in Type 2 Diabetic Patients (Le-Na)

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Rigshospitalet

Status and phase

Completed
Phase 4

Conditions

Weight Gain
Diabetes Type 2

Treatments

Drug: Insulin Detemir, Insulin Insulatard
Drug: Insulin Detemir; Insulin Insulatard

Study type

Interventional

Funder types

Other

Identifiers

NCT00742976
EudraCT 2008-001602-16

Details and patient eligibility

About

Hypothesis: Changing type 2 patients treatment from Insulin Insulatard to Insulin Detemir will increase their excretion of sodium in the urine and thereby decrease their extracellular volume and body weight. 24 patients are divided into 2 groups and their insulin treatment is shifted while their body composition, sodium excretion, weight and extracellular volume is monitored.

Full description

Type 2 diabetic patients experience weight gain when receiving insulin treatment. There has been reports that the weight gain is less or absent when patients are treated with Insulin Detemir. Patients with diabetes have increased total body sodium and increased extracellular volume. We hypothesize that part of the weight gain seen is due to increase in extracellular volume and that the lesser weight gain seen in patients treated with Detemir is due to an lesser increase in extracellular volume. We believe that the cause of this difference is the different pharmacokinetic properties of insulin Detemir. Insulin Detemir i protein bound and is therefore not excreted in the kidneys. This may cause less sodium reabsorption, than with other insulins, and therefore less increase in extracellular volume.

We test this hypothesis by examining urinary sodium excretion, extracellular volume by GFR measurements, Body composition by DEXA scan, body weight, and 24 hour blood pressure.In patients that are changed from Insulin Insulatard to Insulin Detemir and back.

Enrollment

24 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Type 2 diabetes according to WHO 1999 criteria for at least 3 month
  • Insulin treated for at least 1 month
  • BMI 25-40
  • Age 18-80
  • Hb1Ac < 10%

Exclusion criteria

  • Hypertension not well regulated
  • Serum creatinine > 130 micromol/l
  • Non-diabetic kidney disease
  • Disease that may cause invalid hgbA1c measurement
  • Substance abuse
  • Recent use of Detemir
  • Pregnancy or risk of becoming pregnant
  • Any condition that may disturb protocol adherence (language barrier etc) urinary albumin > 30 mg/24hours ( before screening)
  • Use of drugs that may influence blood glucose (except oral antidiabetics)
  • Use of drugs that may influence sodium balance,i.e diuretics ( tiazides accepted)
  • Clinical significant disease that may influence outcome ( cancer etc)

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

24 participants in 2 patient groups

1
Active Comparator group
Description:
8 weeks of insulin Detemir, then cross over to 8 Weeks of Insulatard, then cross over to 1 week of Detemir
Treatment:
Drug: Insulin Detemir, Insulin Insulatard
2
Active Comparator group
Description:
8 weeks of Insulin Insulatard, then cross over to 8 weeks of insulin Detemir, then crossover to 1 week of Insulin Insulatard
Treatment:
Drug: Insulin Detemir, Insulin Insulatard
Drug: Insulin Detemir; Insulin Insulatard

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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