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FDG-PET CT scan: an additional tool in detection of peripheral arterial disease and its compensatory capacities in patients with diabetes type 2, an observational pilot study.

FDG-PET CT scan: an additional tool in detection of peripheral arterial disease and its compensatory capacities in patients with diabetes type 2, an observational pilot study. - FDG-PET scan in peripheral arterial disease in diabetes type 2

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON33453
Enrollment
14
Registered
2009-03-23
Start date
2009-03-01
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

atheroslerosis peripheral arterial disease

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: type 2 diabetes, presence of an threatened distal circulation no smoking.

Exclusion criteria

Exclusion criteria: pregnancy or an actual wish for pregnancy lactation period less than a year in the postmenopausal state HbA1c > 11% at random glucose level more than 12 mmol/l at time of FGDPET scan.

Design outcomes

Primary

MeasureTime frame
1. Assessment of FDG uptake by PET imaging along plaques in the distal vasculature of the lower limbs that is compared with presence of atherosclerotic lesions within the same individual (as determined by conventional CT scanning). 2. Difference in the distribution of FDG uptake by endothelium (at baseline vs. after temporary occlusion by use of a tourniquet for 3 minutes) for each predefined segment along the distal vasculature.

Secondary

MeasureTime frame
1. To evaluate whether FDG uptake significantly correlates to vascular plaques on CT 2. To evaluate whether a FDG PET-derived ischemic border zone correlate with conventional clinical scores of ischemia

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)