This Study is a Prospective, Multi-center, Real World, Observational Study, Which Aims at Evaluating Intermediate and Long-term Efficacy of Endovascular Treatment for TASC C&D Aortoiliac Occlusive Disease.

Sponsor
Shanghai Zhongshan Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05391815
Collaborator
RenJi Hospital (Other), First Affiliated Hospital of Zhejiang University (Other), Chengdu University of Traditional Chinese Medicine (Other), Xuanwu Hospital, Beijing (Other), First People's Hospital of Hangzhou (Other), Qingdao Hiser Medical Group (Other), Second Affiliated Hospital of Soochow University (Other), Liyuan Hospital of Tongji Medical College of Huazhong University of Science and Technology (Other), Huashan Hospital (Other)
800
1
134
6

Study Details

Study Description

Brief Summary

This study is a prospective, multi-center, real world, observational study, which aims at evaluating the intermediate and long-term efficacy of endovascular treatment for TASC C&D aortoiliac occlusive disease .It is estimated that 800 subjects diagnosed with TASC C&D aortoiliac occlusive disease and receive endovascular treatments will be enrolled in nine centers from April 2021 to June 2027 nation-widely. All the subjects will be under follow-up for 60 months. There is no restriction on the endovascular techniques. The primary outcomes covers freedom from TLR at 60 months.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    In the past decade, endovascular treatment has become the first-line treatment for iliac artery occlusion, while Aorta - bilateral femoral artery bypass surgery is preferred for more complex iliac artery occlusion. However, recently, with advances in endovascular devices and techniques, endovascular interventions have gradually replaced open surgery in many clinical problems and have shown ideal safety and efficacy.

    Currently, the optimal treatment for TASC, C&D iliac artery occlusion is controversial, mostly based on limited data from single centers and few large multicenter databases or registries. In addition, the long-term efficacy of stents implantation in iliac artery disease remind unknown and might be influenced by stent type and calcification. Therefore, the purpose of this study was to evaluate the long-term efficacy and safety of endovascular treatment for TASC, C&D iliac artery occlusion in a multicenter study.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    800 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Intermediate and Long-term Efficacy of Endovascular Treatment for TASC C&D Aortoiliac Occlusive Disease: a Prospective, Multicenter, Real-world, Registry Study
    Actual Study Start Date :
    Apr 1, 2021
    Anticipated Primary Completion Date :
    Jun 1, 2027
    Anticipated Study Completion Date :
    Jun 1, 2032

    Outcome Measures

    Primary Outcome Measures

    1. Freedom from clinically-driven TLR [60 months]

      CD-TLR was defined as any reintervention within the target lesion(s) because of recurrent symptoms. Freedom form CD-TLR were defined as the rates of the number of patients who did not receive reintervention verse the number of patients during the follow-up period.

    Secondary Outcome Measures

    1. Technical success rate [30 days]

      We defined the technical success rate as the rate of patients in whom the endovascular treatments are successfully performed.

    2. Incidence of major adverse events. [1month, 3 months,6 months, 12 months ,24 months]

      Major adverse events include anyone of the following: all-cause mortality, Myocardial infarction, ischemic stroke, acute limb ischemia, and major amputation of a vascular etiology, and arterial thrombosis related to endovascular manipulation.

    3. Adverser events related to insufficient lower limb blood supply. [1 month, 3 months, 6 months, 12 months, 24 months, 36 months, 48 months, 60 months]

      Major amputation, acute re-occlusion, subacute re-occlusion and chronic re-occlusion.

    4. CD-TLR [1 month, 3 months, 6 months, 12 months, 24 months, 36 months]

      CD-TLR was defined as any reintervention within the target lesion(s) because of recurrent symptoms.

    5. Vascular quality of life questionnaire(VascuQol) [1 month, 3 months, 6 months, 12 months, 24 months, 36 months, 48 months, 60 months]

      The VascuQol was designed as a questionnaire containing five domains: pain (4 items), symptoms (4 items), activities (8 items), social (2 items), and emotional (7 items) to evaluate Health related quality of life (HRQL). Every item has seven response options, with scores ranging from 1 to 7. A total score is the sum of all 25 item scores divided by 25.And both the total score as well as the domain scores range from 1 (worst HRQL) to 7 (best HRQL).The lower the value, the poorer the quality of life.

    6. Health economics evaluation [60 months]

      All the cost related to the target vessel and spent in the inpatient ward will be recorded and analyzed.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Rutherford grades 3-6.

    2. Follow the follow-up arrangement.

    3. Age: 18-80 years old.

    4. The target lesions were in the lower abdominal aorta and/or the common iliac artery and/or the external iliac artery.

    5. The stenosis degree ≥50%, or restenosis (received PTA or other adjuvant therapy, including bare or covers stents), or complete occlusion, or the presence of aortailiac artery thrombosis after PMT or CDT thrombus clearance, and then further endovascular therapy perfomred.

    6. Signed informed consent.

    Exclusion Criteria:
    1. Known allergy to drugs used in this study, including antiplatelet or anticoagulant drugs, etc.

    2. Allergy to iodine contrast agent allergy;

    3. Coagulation dysfunction or hypercoagulability;

    4. Breast-feeding or pregnant women;

    5. Life expectancy < 24 months;

    6. Body condition can not tolerate endovascular treatment;

    7. Type 2B, type 3 lower limb ischemia patients

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Zhongshan Hospital, Fudan University Shanghai China

    Sponsors and Collaborators

    • Shanghai Zhongshan Hospital
    • RenJi Hospital
    • First Affiliated Hospital of Zhejiang University
    • Chengdu University of Traditional Chinese Medicine
    • Xuanwu Hospital, Beijing
    • First People's Hospital of Hangzhou
    • Qingdao Hiser Medical Group
    • Second Affiliated Hospital of Soochow University
    • Liyuan Hospital of Tongji Medical College of Huazhong University of Science and Technology
    • Huashan Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Shanghai Zhongshan Hospital
    ClinicalTrials.gov Identifier:
    NCT05391815
    Other Study ID Numbers:
    • The ALLIANCE Study
    First Posted:
    May 26, 2022
    Last Update Posted:
    May 26, 2022
    Last Verified:
    May 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Shanghai Zhongshan Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 26, 2022