DIAbetes Maximal ACCeleration (DIAMACC)
Primary Purpose
Peripheral Arterial Disease, Diagnosis, Diabetic Foot
Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Maximal Systolic Acceleration
Sponsored by
About this trial
This is an interventional diagnostic trial for Peripheral Arterial Disease focused on measuring Peripheral Arterial Disease, Diabetic Foot, Diagnosis
Eligibility Criteria
Inclusion Criteria: 18 years or older. DM in medical history. Presenting with a new-onset wound or ulceration on the foot or ankle with initiation of a new diagnostic care path. Exclusion Criteria: - Lacking capacity to consent for inclusion.
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Diagnostic Cohort Study
Arm Description
All patients will underwent full diagnostic testing.
Outcomes
Primary Outcome Measures
Reliability of standard bedside tests and the maximal systolic acceleration (ACCmax)
Sensitivity and specificity including their derivates: PLR and NLR
Secondary Outcome Measures
Comparison of ACCmax reliability with current bedside tests
Comparison of ACCmax reliability with current bedside tests
Comparison of patient demographics (such as age/sex) and comorbidities (duration of diabetes, chronic kidney disease) with diagnostic accuracy of different bedside tests
Comparison of patient demographics (such as age/sex) and comorbidities (duration of diabetes, chronic kidney disease) with diagnostic accuracy of different bedside tests
Wound healing and ACCmax
To assess if the maximal systolic acceleration can predict wound healing
Full Information
NCT ID
NCT05646147
First Posted
November 20, 2022
Last Updated
March 8, 2023
Sponsor
Leiden University Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT05646147
Brief Title
DIAbetes Maximal ACCeleration
Acronym
DIAMACC
Official Title
Diagnostic Accuracy of the Maximal Systolic Acceleration for Detection of Peripheral Arterial
Study Type
Interventional
2. Study Status
Record Verification Date
March 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
July 2023 (Anticipated)
Primary Completion Date
January 2025 (Anticipated)
Study Completion Date
July 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Leiden University Medical Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Prevalence of diabetes mellitus (DM) is increasing rapidly, with patient numbers projected to rise to 643 million by 2030. As a consequence of diabetes-related atherosclerosis, peripheral arterial disease (PAD) and in particular medial arterial calcification (MAC) can occur. The accurate identification of PAD by bedside tests is extremely important in patients with diabetes and foot ulceration, in order to reduce delayed wound healing, prevent lower limb amputation and eventually reduce mortality. However, as shown in previous systematic reviews, the performance of current bedside tests is not reliable in excluding PAD in diabetic patients.1,2 Moreover, the methodological quality of the conducted studies is generally poor. Therefore, more reliable and prospective data is required. Also alternative bedside tests need to be investigated. As an example, the ACCmax (a new doppler derived parameter) could be particularly promising in this patient group.
Detailed Description
According to the latest 2021 data from the International Diabetes Federation, an estimated 537 million adults are living with DM globally.3 Prevalence is increasing rapidly, with numbers projected to rise to 643 million by 2030 and 783 million by 2045. Annually, DM causes 6.7 million deaths, as a consequence of both macrovascular- (atherosclerosis) and microvascular disease (retinopathy, nephropathy, and neuropathy). In 2021, diabetes caused at least 966 billion dollars in health expenditure, comprising approximately 9% of total spending on adults. Type 2 diabetes comprises about 85-90% of these cases, in which disease onset is often insidious, and diagnosis is consequently delayed.4
Peripheral arterial disease (PAD) of the lower extremity is a clinical manifestation of systemic atherosclerosis and considered a well-known (long-term) complication of DM. Besides atherosclerosis, calcification of the tunica media of the arterial wall can occur. This process is called medial arterial calcification (MAC) and is accelerated in the presence of DM. Research suggests that MAC is present in approximately one third of patients with DM.5 MAC has been shown to be an independent predictor of cardiovascular mortality, while another study found that patients with DM and PAD have an impaired quality of life and an increased risk of adverse cardiac and limb events.6,7
Timely recognition of limb ischemia is important in patients with DM/MAC in order to reduce delayed wound healing, prevent lower limb amputation and eventually reduce mortality.8 Current non-invasive bedside tests - such as the ankle-brachial index (ABI) and toe pressure (TP) - are considered accurate for the diagnosis of PAD. However, as shown in previous systematic reviews, the performance of current bedside tests is not reliable in excluding PAD in diabetic patients.1,2 The methodological quality of the studies in these reviews were poor. In general, most of the data was collected retrospectively and not all patients received reference testing. In order to assess the reliability of bedside tests in this patient group, more well-sound methodological research is required. Also alternative bedside tests need to be investigated.
The doppler derived maximal systolic acceleration (ACCmax) is a new non-invasive parameter, which could be promising in detecting PAD. Although ACCmax has already been used for renal artery stenosis9, thorough evaluation has not been performed in PAD. Two previous studies showed accurate diagnostic property in diabetic patients, but the sample sizes were small.10,11
The aim of this study is to assess the clinical value of bedside tests compared to DUS to detect PAD in patients with diabetes-related foot ulceration, with special emphasis on the ACCmax.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Arterial Disease, Diagnosis, Diabetic Foot
Keywords
Peripheral Arterial Disease, Diabetic Foot, Diagnosis
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
238 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Diagnostic Cohort Study
Arm Type
Other
Arm Description
All patients will underwent full diagnostic testing.
Intervention Type
Device
Intervention Name(s)
Maximal Systolic Acceleration
Intervention Description
Reliability of the maximal systolic acceleration
Primary Outcome Measure Information:
Title
Reliability of standard bedside tests and the maximal systolic acceleration (ACCmax)
Description
Sensitivity and specificity including their derivates: PLR and NLR
Time Frame
Through study completion, approximately 1.5 years
Secondary Outcome Measure Information:
Title
Comparison of ACCmax reliability with current bedside tests
Description
Comparison of ACCmax reliability with current bedside tests
Time Frame
Through study completion, approximately 1.5 years
Title
Comparison of patient demographics (such as age/sex) and comorbidities (duration of diabetes, chronic kidney disease) with diagnostic accuracy of different bedside tests
Description
Comparison of patient demographics (such as age/sex) and comorbidities (duration of diabetes, chronic kidney disease) with diagnostic accuracy of different bedside tests
Time Frame
Through study completion, approximately 1.5 years
Title
Wound healing and ACCmax
Description
To assess if the maximal systolic acceleration can predict wound healing
Time Frame
Up to 5 years after study completion
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
18 years or older.
DM in medical history.
Presenting with a new-onset wound or ulceration on the foot or ankle with initiation of a new diagnostic care path.
Exclusion Criteria:
- Lacking capacity to consent for inclusion.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Siem Willems, MD
Phone
+31642642819
Email
s.a.willems@lumc.nl
12. IPD Sharing Statement
Plan to Share IPD
No
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DIAbetes Maximal ACCeleration
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