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Cardiovascular Risk in Peripheral Artery Disease Patients Undergoing Endovascular Revascularisation (RISK)

2026년 5월 13일 업데이트: Martina Turk Veselič, University Medical Centre Ljubljana

Prognostic Markers of Cardiovascular Risk in Peripheral Artery Disease Patients Undergoing Endovascular Revascularisation

This study will investigate heart-related complications in patients with peripheral arterial disease (PAD) undergoing endovascular revascularization procedures to improve blood flow in the legs. Previous studies have shown that some patients develop silent heart injury after these procedures, even without symptoms, and that this may be associated with worse long-term outcomes.

Approximately 500 patients will be included in the study. Blood tests for cardiac biomarkers, including high-sensitivity troponin and NT-proBNP, will be performed before and after the procedure. Participants will also undergo ultrasound examination of the heart to assess heart function, including advanced measures that may detect early or subtle heart damage. In addition, heart rate variability will be measured using a short electrocardiogram recording.

Patients will be followed for 30 days and 1 year after the procedure to assess the occurrence of major cardiovascular events, limb-related complications, and death. Additional blood samples will be collected and stored for future analysis of inflammation, oxidative stress, and genetic markers that may help explain the mechanisms associated with heart injury and prognosis in these patients.

연구 개요

상세 설명

According to the recommendations of the European Society of Cardiology, serial measurement of cardiac troponin before and after procedures with moderate or high peri-procedural risk is recommended in cardiovascular patients undergoing surgery or interventions, including lower extremity revascularization procedures. Peri-operative myocardial infarction/injury (PMI) is defined as an increase in troponin levels on postoperative day 1 or 2 above the reference range compared with the pre-procedural value. Most patients with PMI do not present with typical ECG changes or clinical symptoms suggestive of myocardial ischemia. Identification of PMI is clinically important, as studies have shown that PMI predicts worse cardiovascular outcomes. Patients with PMI have higher 30-day and 1-year mortality rates and a higher incidence of major adverse cardiovascular events. The incidence of PMI in patients with peripheral arterial disease (PAD) is approximately 20%, which is higher than that observed after non-cardiac surgery in the general population.

Only two studies have reported myocardial injury after endovascular revascularization treatment for peripheral arterial disease, specifically myocardial injury after non-cardiac surgery (MINS), which, unlike PMI, excludes non-ischemic causes. In patients with critical limb ischemia, PMI occurred in 25.5% of patients after the procedure and was associated with a 2.4-fold increase in mortality and a 2.9-fold increase in major adverse cardiovascular events within one year. In patients with intermittent claudication, PMI occurred in 2% of patients and was likewise associated with a worse prognosis, with a higher incidence of cardiac death, myocardial infarction, and urgent revascularization during a 2.4-year follow-up period (7% vs. 30.8%).

Current risk assessment recommendations prior to revascularization procedures also include measurement of BNP or NT-proBNP (N-terminal pro-B-type natriuretic peptide). Elevated levels are associated with poorer cardiovascular prognosis and may additionally help identify previously undiagnosed heart failure in patients with PAD. Previous studies have shown NT-proBNP to be a better predictor of perioperative cardiovascular risk than parameters obtained from standard echocardiographic examination.

However, emerging evidence suggests that newer and more advanced echocardiographic parameters, capable of detecting subclinical myocardial dysfunction, may provide additional prognostic value in cardiovascular risk stratification. In patients undergoing major non-cardiac surgery under general anesthesia, impaired preoperative left ventricular global longitudinal strain (LVGLS) demonstrated independent and incremental prognostic value for predicting mortality, acute coronary syndrome, and MINS within 30 days after surgery, whereas left ventricular ejection fraction did not.

Prognostic assessment in patients with PAD may potentially be further improved by evaluation of myocardial work (MW) echocardiographic parameters, although data on this topic are currently lacking. Furthermore, it remains unknown whether endovascular revascularization procedures influence heart rate variability (HRV), which is also an established prognostic marker.

We plan to enroll approximately 500 patients with PAD admitted to the Department of Vascular Diseases for endovascular revascularization treatment. In accordance with ESC recommendations, NT-proBNP levels will be measured at admission, while high-sensitivity cardiac troponin T/I (hs-cTnT/I) will be measured at admission and on the day after the procedure to assess the incidence of PMI. Participants will also undergo transthoracic echocardiography, primarily for assessment of LVGLS and myocardial work parameters. In addition, heart rate variability will be assessed before and after the procedure using a 5-minute high-resolution ECG recording (Cardiax device) obtained in the supine position.

At 30 days and 1 year after the procedure, the following primary outcomes will be recorded:

  • Major adverse cardiovascular events (MACE), defined as a composite endpoint of myocardial infarction, stroke, unstable angina, or cardiovascular death;
  • Major adverse limb events (MALE), defined as a composite endpoint of untreated loss of patency of the revascularized segment, repeat intervention on the revascularized segment, or above- or below-knee amputation of the revascularized limb;
  • All-cause mortality. To enable future investigation of the potential mechanisms underlying the observed results, additional blood samples will be collected before and after the procedure for analysis of inflammatory and oxidative stress biomarkers. Furthermore, an additional preprocedural blood sample will be collected for genetic biomarker analysis. These samples will be stored frozen for subsequent analysis.

연구 유형

관찰

등록 (추정된)

500

연락처 및 위치

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연구 장소

      • Ljubljana, 슬로베니아, 1000
        • University Medical Centre Ljubljana

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 어린이
  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

샘플링 방법

비확률 샘플

연구 인구

The study population will consist of approximately 500 adult patients with Peripheral Arterial Disease who are admitted to the University Medical Centre Ljubljana for elective or urgent endovascular revascularization treatment of lower extremity peripheral arterial disease, including patients with intermittent claudication and chronic limb-threatening ischemia. Participants will be recruited consecutively during hospitalization and enrolled after providing written informed consent.

설명

Inclusion Criteria:

  • Patients with Peripheral Arterial Disease admitted to the University Medical Centre Ljubljana for endovascular treatment of lower extremity peripheral arterial disease.
  • Ability and willingness to provide written informed consent after explanation of the purpose and procedures of the study.

Exclusion Criteria:

  • Active malignant disease.
  • End-stage renal disease requiring dialysis treatment.
  • Previous enrollment in the study.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

코호트 및 개입

그룹/코호트
peripheral arterial disease patients
peripheral arterial disease patients following endovascular revascularization procedure

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Major adverse cardiovascular events (MACE)
기간: 30 days and 1 year after the procedure
composite endpoint of myocardial infarction, stroke, unstable angina, or cardiovascular death
30 days and 1 year after the procedure
Major adverse limb events (MALE)
기간: 30 days and 1 year after the procedure
composite endpoint of untreated loss of patency of the revascularized segment, repeat intervention on the revascularized segment, or above- or below-knee amputation of the revascularized limb
30 days and 1 year after the procedure
All-cause mortality
기간: 30 days and 1 year after the procedure
death from any reason
30 days and 1 year after the procedure

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2025년 2월 12일

기본 완료 (추정된)

2027년 3월 30일

연구 완료 (추정된)

2027년 12월 30일

연구 등록 날짜

최초 제출

2026년 5월 13일

QC 기준을 충족하는 최초 제출

2026년 5월 13일

처음 게시됨 (실제)

2026년 5월 20일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 5월 20일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 5월 13일

마지막으로 확인됨

2026년 5월 1일

추가 정보

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개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

IPD 계획 설명

lack of time resources

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미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

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