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The Microvascular Function of GLP-1 and Its Analogues

K

Katarina Kos

Status

Completed

Conditions

Obesity
Type 2 Diabetes

Treatments

Drug: GLP-1
Drug: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT01677104
1204620 (Other Identifier)
11/SW/0195

Details and patient eligibility

About

Incretins have become a successful drug target in the repertoire of medications used for the treatment of type 2 diabetes. However little is known about a potential benefit of GLP-1 on the vascular system in humans, independent of their glucose lowering actions and data are only derived from ex vivo studies in animals. Particularly little is known about clinically relevant benefits of GLP-1 and its analogues on the microvascular system of individuals with type 2 diabetes.

The vascular effect could be medicated by endogenous GLP-1 (9,36) amide, the breakdown product of GLP-1 (7,36) amide which has a low affinity for the GLP-1 receptor. The investigators hypothesis is that the co-administration of DPP-IV inhibitors will lack the beneficial effects of GLP-1 on the vascular system as GLP-1 (9,36) amide will not be produced by the body.

The study aims to examine the response of GLP-1 and its analogues on small blood vessels and examine the effect of the addition of DPP-IV inhibition in healthy lean individuals, obese individuals and subjects with Type 2 diabetes.

Enrollment

63 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Lean BMI ≤ 25.0 kg/m2
  • Obese BMI ≥30.0kg/m2
  • Non diabetic subjects and subjects with Type 2 diabetes on stable medication for at least 3 months

Exclusion criteria

  • cardiovascular disease
  • Raynaud's disease
  • current treatment with any anti-hypertensive
  • lipid lowering therapies
  • severe hepatic impairment
  • pregnancy and lactation
  • subjects with Type 2 diabetes on insulin therapy
  • subjects with Type 2 diabetes on sulphonylureas
  • subjects with Type 2 diabetes on incretin based therapies
  • subjects with Type 2 diabetes and peripheral vascular disease
  • subjects with Type 2 diabetes and history of advanced retinopathy
  • subjects with Type 2 diabetes and advanced nephropathy
  • subjects with Type 2 diabetes with uncontrolled diabetes (HbA1c > 8.5%)

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

63 participants in 2 patient groups, including a placebo group

DPP-IV inhibitor
Active Comparator group
Description:
Linagliptin 5mg (Tradjenta) before microinjection of GLP-1 and its analogues
Treatment:
Drug: Placebo
Drug: GLP-1
Placebo pill
Placebo Comparator group
Description:
One placebo tablet before microinjection
Treatment:
Drug: Placebo
Drug: GLP-1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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