Outcomes of Straight-line Flow Versus Angiosome-targeted Angioplasty in Treatment of Critical Lower Limb Ischemia

Sponsor
Kafrelsheikh University (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT06127134
Collaborator
(none)
100
1
2
12
8.3

Study Details

Study Description

Brief Summary

Peripheral arterial disease (PAD) affects more than 200 million people worldwide. Although over 50% are asymptomatic, it accounts for 4% of all amputations.

The ischemic limb must be revascularized to help wound healing, reduce the pain of ischemia and preserve the limb's function. So, surgical and percutaneous revascularization choices must be considered in CLI. Classically, CLI revascularization aims to provide at least one patent vessel that delivers in-line flow to the foot.

Today, the investigators live in a new era of angioplasty evolving and substituting open vascular surgery, so expanding research on endovascular strategy has been noticed.This confirms the profound impact of angioplasty in vascular surgery as one of the fastest-growing branches of medicine

Infrapopliteal artery occlusive disease (IPOD) is a significant cause of critical limb-threatening ischemia (CLTI). The worldwide prevalence of IPOD is between 4.5% and 29%, and most patients live in low-income countries.

The angiosomal concept was derived from plastic surgery for the skin flap. This concept delineates the human body into three-dimensional blocks of tissue from the skin to bone and also provides practical application of vascular anatomy for reconstructive surgery. An angiosome is an anatomic unit of tissue consisting of skin, subcutaneous, muscle, and bone fed by a source artery and drained by a specific vein.

According to the angiosomal concept, the foot is divided into six distinct angiosomes fed by source arteries, three from the posterior tibial, two from the peroneal, and one from the anterior tibial artery, with functional artery-to-artery connections among muscle, fascia, and skin. Numerous direct inter-arterial connections occur between the foot's main arteries, which provide alternative pathways of blood flow when disruption or compromise affects the arteries that directly feed the angiosome.

On the other hand, in patients with CLI, where only one vessel runoff can be established to the foot, direct flow into a patent pedal arch is essential to improve their clinical outcomes.

Conventional Endovascular therapy aims to the re-establishment of pulsatile straight-line flow to the lower limb. This results in relieving ischemic pain, healing ulcers, achieving limb salvage, improving quality of life, and potentially prolonging survival.

So it became essential to know the differential impact of both concepts on CLI revascularization.

Condition or Disease Intervention/Treatment Phase
  • Procedure: peripheral angioplasty for tibial vessels
N/A

Detailed Description

Introduction

Peripheral arterial disease (PAD) affects more than 200 million people worldwide. Although over 50% are asymptomatic, it accounts for 4% of all amputations.

The ischemic limb must be revascularized to help wound healing, reduce the pain of ischemia and preserve the limb's function. So, surgical and percutaneous revascularization choices must be considered in CLI. Classically, CLI revascularization aims to provide at least one patent vessel that delivers in-line flow to the foot.

Today, the investigators live in a new era of angioplasty evolving and substituting open vascular surgery, so expanding research on endovascular strategy has been noticed.This confirms the profound impact of angioplasty in vascular surgery as one of the fastest-growing branches of medicine

Infrapopliteal artery occlusive disease (IPOD) is a significant cause of critical limb-threatening ischemia (CLTI). The worldwide prevalence of IPOD is between 4.5% and 29%, and most patients live in low-income countries.

The angiosomal concept was derived from plastic surgery for the skin flap. This concept delineates the human body into three-dimensional blocks of tissue from the skin to bone and also provides practical application of vascular anatomy for reconstructive surgery. An angiosome is an anatomic unit of tissue consisting of skin, subcutaneous, muscle, and bone fed by a source artery and drained by a specific vein.

According to the angiosomal concept, the foot is divided into six distinct angiosomes fed by source arteries, three from the posterior tibial, two from the peroneal, and one from the anterior tibial artery, with functional artery-to-artery connections among muscle, fascia, and skin. Numerous direct inter-arterial connections occur between the foot's main arteries, which provide alternative pathways of blood flow when disruption or compromise affects the arteries that directly feed the angiosome.

On the other hand, in patients with CLI, where only one vessel runoff can be established to the foot, direct flow into a patent pedal arch is essential to improve their clinical outcomes.

Conventional Endovascular therapy aims to the re-establishment of pulsatile straight-line flow to the lower limb. This results in relieving ischemic pain, healing ulcers, achieving limb salvage, improving quality of life, and potentially prolonging survival.

So it became essential to know the differential impact of both concepts on CLI revascularization.

Aim of the work Comparing the efficiency of two percutaneous transluminal angioplasty techniques for Critical Lower Limb Ischemia revascularization, Straight-line flow (Group A) versus Angiosome-targeted (Group B).As regard short-term impact.

Patient and methods

  1. Study Ethics the investigators will conduct this study after the approval of the I.R.B. (Institutional Review Board) of Kafrelsheikh University Hospital. All included procedures will be according to the Declaration of Helsinki. the investigators will also obtain the patients' informed consent to use their data in their research. All evaluation forms, reports, and other records that leave the site would not include unique personal data to maintain subject confidentiality.

  2. Study design: a non-randomized clinical trial.

  3. Time of study: The study will be conducted in 2023.

  4. all patients will be submitted to the following preoperative evaluation : 1-History : 1. Personal data. 2. Risk factors: smoking, DM, hypertension, hypercholesterolemia. 3. Co-morbidity: previous stroke, angina, MI, and CKD. 4. Previous PAD interventions to one or both legs. 5. Previous amputations. 6. Previous coronary intervention (CABG, PCI) 2-

Physical examination, including:
  1. Assessment of functional status: independent stick walker, prosthesis, wheelchair, bed-bound 2. Recording of peripheral pulses 3. Measurement of ABPI or TBPI 4. Wound assessment (in those patients with tissue loss) 5. Assessment of ischaemic night/rest pain. 3-Investigations: A) Laboratory

  2. Routine hematology (hemoglobin, white cell count, platelet count, HbA1c)

  3. Routine biochemistry (creatinine, estimated GFR, ESR, CRP, RBS, cholesterol, HBA1c)

  4. PT, PTT, INR

  5. Lipid profile.

B)Imaging of their arteries by one or more of the following modalities:
  1. Duplex ultrasound.

  2. Computerized tomography angiography (CTA)

  3. Magnetic resonance angiography (MRA)

  4. Digital subtraction angiography (DUS)

(5) Patients with critical lower limb ischemia are going to be classified according to

• Modified TASC II classification 2016 (Trans-Atlantic Inter-society Consensus), which is a morphological classification

• Rutherford classification, which is the clinical classification

(6) Surgical procedure. Therapeutic intervention (angioplasty)

(7) Post-operative follow-up.

Follow-up of the patients will be at the first, third, and sixth months from the intervention date. Progress of limb conditions after the intervention will be observed which will be regarding :

  • Diminution or absence of rest pain

  • Healing of ulcers.

  • limb salvage Assessed by Visual Analogue Scale (VAS)

  • complications

(8) Sampling technique:

The sample size of 100 patients classified into two groups

(9) Statistical analysis:

Analysis of data will be done using SPSS (statistical package for social science)

(10) Inclusion Criteria:

  • Patient with documented symptomatic infragenicular chronic arterial disease with or without supra-genicular lesion

  • Diabetic or not

  • Rutherford grades 4, 5 and 6

  • The patient is able and willing to comply with study follow-up requirements.

(11) Exclusion Criteria:

  • Contraindication for angioplasty

  • unsuitable for angioplasty revascularization strategy

  • claudication case

  • tissue loss is considered to be primarily of venous etiology.

  • Patient with full-thickness gangrene of the foot.

  • Widespread infection of the lower limb needing amputation

(12) Outcome Measures :

  • Technical success as documented by angiography pre & post procedure with residual stenosis <30%

  • Clinical success is improving at least one class in Rutherford classification in patients with chronic limb ischemia.

  • Primary patency at six months follow-up.

  • Successful target lesion revascularization.

  • The absence of major adverse events is defined as unplanned major amputation of the index limb.

  • Absence of non-managed complications

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Outcomes of Straight-line Flow Versus Angiosome-targeted Angioplasty in Treatment of Critical Lower Limb Ischemia
Actual Study Start Date :
Jan 1, 2023
Anticipated Primary Completion Date :
Nov 15, 2023
Anticipated Study Completion Date :
Jan 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Straight-line flow (Group A)

treating less diseased arteries which is in line with distal run off the foot

Procedure: peripheral angioplasty for tibial vessels
repair tibials blood vessels throughout two concepts using angioplasty ballooning
Other Names:
  • endovascular arterial repair for critical lower limb ischemia
  • Sham Comparator: Angiosome-targeted (Group B)

    treating specific angiosome through a targeted vessel which mainly supplies this angiosome

    Procedure: peripheral angioplasty for tibial vessels
    repair tibials blood vessels throughout two concepts using angioplasty ballooning
    Other Names:
  • endovascular arterial repair for critical lower limb ischemia
  • Outcome Measures

    Primary Outcome Measures

    1. Technical success [first 24 hours]

      good distal flow and arterial pulsation which are documented by angiography pre & post procedure with residual stenosis <30%

    2. Clinical success [first 6 month]

      limb salvage and wound status improves at least one class in Rutherford classification in patients with critical limb ischemia.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patient with documented symptomatic infragenicular chronic arterial disease with or without supra-genicular lesion

    • Diabetic or not

    • Rutherford grades 4, 5 and 6

    • The patient is able and willing to comply with study follow-up requirements.

    Exclusion Criteria:
    • Contraindication for angioplasty

    • unsuitable for angioplasty revascularization strategy

    • claudication case

    • tissue loss is considered to be primarily of venous etiology.

    • Patient with full-thickness gangrene of the foot.

    • Widespread infection of the lower limb needing amputation

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Kafrelsheikh University Kafr Ash Shaykh Egypt

    Sponsors and Collaborators

    • Kafrelsheikh University

    Investigators

    • Principal Investigator: Ahmed M Bedeer, MD, KFS university

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ahmed Mohamed Elsaid Hassan Bedeer, Principal Investigator, Kafrelsheikh University
    ClinicalTrials.gov Identifier:
    NCT06127134
    Other Study ID Numbers:
    • MSKU 50-2-28
    First Posted:
    Nov 13, 2023
    Last Update Posted:
    Nov 14, 2023
    Last Verified:
    Nov 1, 2023
    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 Ahmed Mohamed Elsaid Hassan Bedeer, Principal Investigator, Kafrelsheikh University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 14, 2023