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Effects of Acarbose on Endothelial Function After a Mixed Meal in Newly Diagnosed Type 2 Diabetes

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00551954
Enrollment
Unknown
Registered
2007-11-01
Start date
2006-07-31
Completion date
Unknown
Last updated
2013-03-01

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

Conditions

Type 2 Diabetes

Brief summary

Endothelial dysfunction (ED) has been suggested as a possible causal link between postprandial hyperglycemia and cardiovascular events in patients with type 2 diabetes. Recent trials demonstrated a reduction of cardiovascular events by treatment with the alpha glucosidase inhibitor acarbose - a drug which mainly reduces postprandial glucose excursions. We were interested whether patients with newly diagnosed type 2 diabetes showed postprandial ED and if so whether acarbose was able to improve this condition.

Interventions

DRUGacarbose

100 mg (tablets) t.i.d.

DRUGplacebo

one tablet t.i.d.

Sponsors

Technische Universität Dresden
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
35 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* age 35-75 years * type 2 diabetes (newly diagnosed) * well glycemic control (HbA1c \</= 8.1) * leucocyte count \> 6.2 or hs CrP \> 1

Exclusion criteria

* hs CrP \> 10 * type 1 diabetes * previous treatment with antidiabetic drugs

Design outcomes

Primary

MeasureTime frame
forearm blood flow assessed by forearm occlusion plethysmography after a mixed mealat baseline and after 20 weeks of treatment

Secondary

MeasureTime frame
forearm blood flow assessed by forearm occlusion plethysmography in the fasting state, plasma glucose excursion in response to the mixed meal, insulin levels in response to the mixed meal, triglyceride levels in response to the mixed mealat baseline and after 20 weeks of treatment

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026