search
Back to results

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
Leiden University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Peripheral Arterial Disease focused on measuring Peripheral Arterial Disease, Diabetic Foot, Diagnosis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    November 20, 2022
    Last Updated
    March 8, 2023
    Sponsor
    Leiden University Medical Center
    search

    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

    Learn more about this trial

    DIAbetes Maximal ACCeleration

    We'll reach out to this number within 24 hrs