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The Microvascular Function of GLP-1 and Its Analogues

The Microvascular Function of GLP-1 and Its Analogues in Humans, in Vivo: the Role of DPP-IV Inhibition

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01677104
Enrollment
63
Registered
2012-08-31
Start date
2012-08-31
Completion date
2014-07-31
Last updated
2017-04-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity, Type 2 Diabetes

Keywords

GLP-1, DPP-IV inhibitor, microcirculation, Exenatide, Liraglutide, Linagliptin

Brief summary

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.

Interventions

DRUGGLP-1

GLP-1 and its analogues will be compared with placebo with and without prior DPP-IV inhibition

DRUGPlacebo

Sponsors

Diabetes UK
CollaboratorOTHER
Katarina Kos
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
DIAGNOSTIC
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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%)

Design outcomes

Primary

MeasureTime frameDescription
skin blood flow3 hoursskin blood flow will be assessed before and after microinjection of GLP-1 or its analogues and the injection site monitored and compared to sites injected with placebo

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026