Skip to main content
Clinical Trials/NCT03295539
NCT03295539UnknownNot Applicable

MulticentRe pOst-market exPeriencE With the INdigo Thrombectomy System for the Treatment of Acute Lower Limb Ischaemia : (Re-Open Registry)

Lancashire Care NHS Foundation Trust1 site in 1 country400 target enrollmentStarted: November 1, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
400
Locations
1
Primary Endpoint
Technical success using the Indigo system.

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Acute lower limb Ischaemia with acute soft clot.

Exclusion Criteria

  • •Calcified plaques/ chronic disease causing critical limb Ischaemia

Arms & Interventions

Acute or Chronic clot

Other

If chronic clot, no intervention given via Indigo

Intervention: 'Indigo' Mechanical thrombectomy system (Device)

Outcomes

Primary Outcomes

Technical success using the Indigo system.

Time Frame: Time to event anaylsis. Primary patency results are immediate after the case on the final angiogram images.

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 Outcomes

No secondary outcomes reported

Investigators

Sponsor
Lancashire Care NHS Foundation Trust
Sponsor Class
Network
Responsible Party
Principal Investigator
Principal Investigator

Bella Huasen

Endovascular Interventional Consultant

Lancashire Care NHS Foundation Trust

Study Sites (1)

Loading locations...

Similar Trials