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Laboratory, Cellular and Molecular Determinants of Clinical Success in Diabetic Patients With Critical Limb Ischemia

Prospective Evaluation of Laboratory, Cellular and Molecular Determinants of Clinical Success of the Treatment in Diabetic Patients With Critical Limb Ischemia (ECAD-CLI) Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03636867
Acronym
ECAD-CLI
Enrollment
236
Registered
2018-08-17
Start date
2018-08-07
Completion date
2020-08-31
Last updated
2023-03-24

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

Conditions

Critical Limb Ischemia, Critical Lower Limb Ischemia, Diabetes Mellitus, Diabetic Foot

Brief summary

The ECAD-CLI is an investigator-driven, prospective, single-center study. The aim of the study is to prospectively collect clinical, laboratory, angiographic, cellular and molecular variables related to prognosis and outcome in patients with diabetes mellitus and critical limb ischemia.

Detailed description

All consecutive patients admitted to Maria Cecilia Hospital will be enrolled in the ECAD-CLI study. According to interventional management of the patient the following data and samples will be prospectively collected and related to outcome: * medical history, cardiovascular risk factors, clinical presentation * information related to angiography of peripheral arteries. An independent core-lab will review angiographies to assess extent and severity of peripheral artery disease * information related to medical treatment, including antithrombotic agents, antimicrobics and any treatment to permit wound healing * blood sample to obtain DNA, RNA and serum * patient undergoing surgery and/or debridement for wound/ulcer due to diabetic foot disease will receive biopsy for specimen collection * atherosclerotic plaque sample in patients undergoing atherectomy for the treatment of the peripheral artery disease All clinical variables and information obtained from blood/tissue samples will be related to outcome. Any adverse events will be judged by an independent blinded committee.

Interventions

to identify laboratory, cellular and molecular determinants of clinical success after treatment, several clinical information and specimens will be collected by Authors from each patient

Sponsors

Maria Cecilia Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* diagnosis of diabetes mellitus in treatment with oral agents and/or insulin * diagnosis of critical limb ischemia requiring medical and/or interventional treatment

Exclusion criteria

* dialysis * diagnosis or suspicion of malignancy * life expectancy \<1 year * inability to guarantee clinical follow-up

Design outcomes

Primary

MeasureTime frameDescription
Incidence of amputation1-yearOccurrence of major or minor amputation

Secondary

MeasureTime frameDescription
Wound healing1-yearoccurrence of wound healing
Change in WIfI class1-yearThe Wound, Ischemia and Foot Infection is the most used classification for patients with diabetic foot disease. The classification ranges from 0 to 9. The scale includes 3 items: wound extension, presence and severity of ischemia, presence and severity of ischemia. Each item ranges from 0 to 3 points.
Change in Rutherford class1-yearThe Rutherford classification is the most used scale to stratify patients with peripheral artery disease. The classification ranges from class I to class VI. Patients with critical limb ischemia show a class from IV to VI. The Rutherford class will be assessed in all patients at baseline and 1-year after to estimate the presence or not of improvement
Incidence of revascularization of peripheral arteries1-yearany procedure (percutaneous or surgical) of revascularization of peripheral arteries

Other

MeasureTime frameDescription
Incidence of major cardio and cerebrovascular adverse events (MACCE)1-yearcumulative occurrence of all-cause death, myocardial infarction, cerebrovascular accident

Countries

Italy

Outcome results

None listed

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