Acute Limb Ischaemia (ALI) Management With 'Indigo' Mechanical Aspiration System
Primary Purpose
Lower Limb Ischemia
Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
'Indigo' Mechanical thrombectomy system
Sponsored by

About this trial
This is an interventional treatment trial for Lower Limb Ischemia
Eligibility Criteria
Inclusion Criteria:
- Acute lower limb Ischaemia with acute soft clot.
Exclusion Criteria:
- Calcified plaques/ chronic disease causing critical limb Ischaemia
Sites / Locations
- Interventional Radiology
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Acute or Chronic clot
Arm Description
If chronic clot, no intervention given via Indigo
Outcomes
Primary Outcome Measures
Technical success using the Indigo system.
Intraoperative technical success defined as the restoration of antegrade blood flow with complete or near complete (95% by volume) removal of the thrombus or embolus (70% threshold). This is assessed using imaging modalities (USS/Doppler/Fluroscopy) and clinical assessment of the affected limb.
See for this definition the enclosed citation. In conclusion, the primary outcome measure will be improvement in blood flow across a lesion assessed by the improvement in Thrombolysis in Myocardial Infarction (TIMI) score that was adapted to peripheral arteries. Concomitant balloon angioplasty or stent placement in addition to VAT was considered a complementary treatment. Additional thrombectomy treatments, such as thrombolysis and mechanical thrombectomy, were considered technical failures.Target lesions were grouped anatomically into above-the-knee(ATK) or below-the-knee(BTK) lesions.
Secondary Outcome Measures
Full Information
NCT ID
NCT03295539
First Posted
September 6, 2017
Last Updated
October 19, 2017
Sponsor
Lancashire Care NHS Foundation Trust
Collaborators
St. Franziskus Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03295539
Brief Title
Acute Limb Ischaemia (ALI) Management With 'Indigo' Mechanical Aspiration System
Official Title
MulticentRe pOst-market exPeriencE With the INdigo Thrombectomy System for the Treatment of Acute Lower Limb Ischaemia : (Re-Open Registry)
Study Type
Interventional
2. Study Status
Record Verification Date
October 2017
Overall Recruitment Status
Unknown status
Study Start Date
November 1, 2017 (Anticipated)
Primary Completion Date
October 1, 2018 (Anticipated)
Study Completion Date
March 1, 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Lancashire Care NHS Foundation Trust
Collaborators
St. Franziskus Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
International Multi-Centre registry recording comprehensive data on the use of 'Indigo' Mechanical thrombectomy system by Penumbra Inc for the removal of acute clot causing acute or critical limb ischaemia.
Detailed Description
A detailed registry has been designed and approved to be used world wide in vascular and trauma centres, already providing endovascular service for the management of critical limb ischaemia (CLI).
Recent campaigns have shown little is done to improve flow to the lower limbs (legs) of patients to avoid amputation rates. During this time many devises have been used and available on the market. The 'Indigo' system by Penumbra was originally designed from the acute stroke system "ACE". Similar principles were applied in designing the 'Indigo' system. This is currently being used in many centres to manage acute clot causing lower limb ischaemia, however no official registry or international clinical trial has been done to show its significance in managing this disease.
The investigator groups, have created this to come up with enough data to evaluate the Indigo system in the management of (ALI) and offer tips and tricks to other clinicians. The aim is for a single arm, multicenter, retrospective analysis of patients in whom (ALI) was performed with the Penumbra/Indigo System (study device), and gather greater data and information than the PRISM trial in 2013-2014 which obtained only 79 patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lower Limb Ischemia
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
400 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Acute or Chronic clot
Arm Type
Other
Arm Description
If chronic clot, no intervention given via Indigo
Intervention Type
Device
Intervention Name(s)
'Indigo' Mechanical thrombectomy system
Intervention Description
Removal of acute clot from the artery causing ischaemia, using the mechanical aspiration system by Penumbra Inc called "INDIGO"
Primary Outcome Measure Information:
Title
Technical success using the Indigo system.
Description
Intraoperative technical success defined as the restoration of antegrade blood flow with complete or near complete (95% by volume) removal of the thrombus or embolus (70% threshold). This is assessed using imaging modalities (USS/Doppler/Fluroscopy) and clinical assessment of the affected limb.
See for this definition the enclosed citation. In conclusion, the primary outcome measure will be improvement in blood flow across a lesion assessed by the improvement in Thrombolysis in Myocardial Infarction (TIMI) score that was adapted to peripheral arteries. Concomitant balloon angioplasty or stent placement in addition to VAT was considered a complementary treatment. Additional thrombectomy treatments, such as thrombolysis and mechanical thrombectomy, were considered technical failures.Target lesions were grouped anatomically into above-the-knee(ATK) or below-the-knee(BTK) lesions.
Time Frame
Time to event anaylsis. Primary patency results are immediate after the case on the final angiogram images.
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Acute lower limb Ischaemia with acute soft clot.
Exclusion Criteria:
Calcified plaques/ chronic disease causing critical limb Ischaemia
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Bella Huasen, MD
Phone
00447871800565
Email
doctorbella.h@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Theo Bisdas, Phd, MD
Phone
00492519355829
Email
th.bisdas@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bella Huasen, MD
Organizational Affiliation
Lancashire NHS
Official's Role
Study Chair
Facility Information:
Facility Name
Interventional Radiology
City
Preston
State/Province
Lancashire
ZIP/Postal Code
PR2 7HR
Country
United Kingdom
Facility Contact:
First Name & Middle Initial & Last Name & Degree
BELLA HUASEN, MD
Phone
00447871800565
Email
doctorbella.h@gmail.com
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
The registry and data in-put
IPD Sharing Time Frame
while the study is on-going
IPD Sharing Access Criteria
Centres taking part will be given the access via the three main trial investigators Dr Huasen, Dr Bisdas, and Dr Beropoulis
Citations:
PubMed Identifier
21882081
Citation
Karnabatidis D, Spiliopoulos S, Tsetis D, Siablis D. Quality improvement guidelines for percutaneous catheter-directed intra-arterial thrombolysis and mechanical thrombectomy for acute lower-limb ischemia. Cardiovasc Intervent Radiol. 2011 Dec;34(6):1123-36. doi: 10.1007/s00270-011-0258-z. Epub 2011 Sep 1.
Results Reference
result
Learn more about this trial
Acute Limb Ischaemia (ALI) Management With 'Indigo' Mechanical Aspiration System
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