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CompletedNCT00832741Updated Jan 30, 2009

Incretin Hormones in Type-1 Diabetes Mellitus Glycemic Response in Type-1 Diabetes Mellitus

An observational study in Type 1 Diabetes, sponsored by Hvidovre University Hospital. Completed at 1 site in Denmark. Open to participants aged 18 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2009-01-30.

Sponsored by Hvidovre University Hospital · Observational

Study type
Observational
Enrollment
30
Ages
18 Years to 60 Years
Sex
All
01

Study summary

The purpose of this study is to investigate whether secretion of incretin hormones is intact and to what extent endogenous as well as exogenous GLP-1 controls postprandial glucose excursions in patients with type-1 diabetes mellitus.

Read the detailed description

GLP-1 and GIP are incretin hormones secreted from specific endocrine celles in the gut. Stimulus for secretion is prescence of carbohydrates, fat and protein in the gut. The incretin hormones controls postprandial glucose excursions through stimulation of insulinsecretion as well as inhibition of glucagon and gastric emptying.The effects of GLP-1 on insulin secretion and glucagon inhibition are glucose dependent and the risc of hypoglycemia is therefore negligible when the hormone is administered in supra physiological concentrations.Furthermore, some animal studies suggest that GLP-1 has a trofic effect on the betacells and the hormone has been shown to replenish intracellular stores of insulin. Because the main bloodglucose lowering effect of GLP-1 has been thought to be due to increased insulin secretion, analouges of the hormone has been developed for the treatment of type-2 diabetes. So far, relatively little is known about the effect of GLP-1 in type-1 diabetes.It possible, that GLP-1 in combination with insulin (possibly mainly through its effect on glucagon inhibition and gastric emptying) could reduce the need for exogenous insulin with a concomitant reduced risc of hypoglycemia. Without compromising the target glucemic control. This study focuses of the postprandial bloodglucose lowering effects of endogenous as well as exogenous GLP-1 in patients with type-1 diabetes according to residual betacell function and glycemic control.Furthermore, the endogenous secretion of incretin hormones in patients with type-1 diabetes mellitus will be compared to that of matched normal controls.

02

Conditions studied

  • Type 1 Diabetes

Keywords

  • GLP-1
  • Type 1 diabetes
  • Glycemic control
  • Incretin hormone
03

In context

Diabetes Mellitus

10,925 studies on the registry are indexed under Diabetes Mellitus; 1,319 are open to participants now.

This study's enrollment of 30 is below the median of 233 across 2,220 observational studies indexed under Diabetes Mellitus.

Browse Diabetes Mellitus studies →

Lead sponsor

Hvidovre University Hospital is the lead sponsor of 295 studies on the registry; 21 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

primary care clinic patients and community population(control subjects)

Inclusion criteria

  • type-1 diabetes mellitus
  • diagnosis between 5-40 years.
  • age 18-60 year
  • normal weight at time of diagnosis
  • insulintreatment from diagnosis
  • HbA1c \< 7.6 %

Exclusion criteria

Exclusion Criteria:

  • diabetic complications
  • disease other than type-1 diabetes
05

Study design

Enrollment
30 participants (actual)
Biospecimen retention
Samples with dna
06

What researchers measure

Primary outcomes

  1. blood glucose

    Time frame: 4 hours

Secondary outcomes

  1. GLP-1 and GIP response during a meal

    Time frame: 4 hours

  2. betacell function (incremental area under the c-peptide concentration curve)

    Time frame: 4 hours

  3. alfa cell function (plasma glucagon)

    Time frame: 4 hours

  4. gastric emptying

    Time frame: 4 hours

07

Study locations

1 site
  • Hvidovre University Hospital
    Hvidovre, 2650, Denmark
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 30, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00832741
Lead sponsor
Hvidovre University Hospital
First posted
Jan 30, 2009
Start date
May 2008
Primary completion
Oct 2008
Completion
Oct 2008
Last update
Jan 30, 2009

Study contacts

Urd Kielgast, MD
study director · unafilliated
Sten Madsbad, MD, DMSc
principal investigator · Unafilliated

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2009. You cannot join it, but the record below documents what was studied.

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