Interest of Direct Aspiration First Pass Technique (ADAPT) for Thrombectomy Revascularisation of Large Vessel Occlusion in Acute Ischaemic Stroke

Ischemic Cerebrovascular Accident Clinical Trial

— ASTER  

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02523261
• Other study ID #: MPN_2015_22
• Status: Completed
• Phase: N/A
• First received: August 12, 2015
• Last updated: February 7, 2018
• Start date: October 10, 2015
• Est. completion date: February 2017

Study information

• Verified date: February 2018
• Source: Fondation Ophtalmologique Adolphe de Rothschild
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Mechanical thrombectomy (TM) is now validated through 4 randomized controlled trials of high scientific level as the reference treatment of cerebral infarction associated with proximal cerebral occlusion (MR CLEAN, ESCAPE 2014, 2015). These studies have shown for the first time a major decrease (-35%) of disability related to severe cerebral infarction and reduction in mortality. These studies only used thrombectomy devices called stent retriever for obtaining recanalization rates ranging from 58-72% for the 2 largest studies (MR CLEAN, ESCAPE 2014, 2015). This criterion "recanalization" is important because it largely determines the functional prognosis of patients with severe cerebral infarction (Khatri, 2014).

These results are exciting but we can do even better. Indeed, already new thrombectomy devices are available with a special interest for ADAPT (A Direct Aspiration First Pass Technic). This distal suction system, with a high level of endovascular navigability, provides high recanalization rates (> 90%), low morbidity, with a synergistic effect with stent retriever (Turk A, Kowoll 2014 and 2015). To date, these technic (ADAPT) has never been assessed in a randomized controlled trial.

We have previously conducted a comparative observational study between two recanalization strategies by thrombectomy using first-line ADAPT or the most widely used stent retriever. The interventional neuroradiologist could, in case of recanalization failure with the Solitaire system, used another thrombectomy material left to the operator's choice. 244 consecutive patients on two centers (Rothschild Foundation, and Foch Hospital, France) admitted for a cerebral infarction associated with proximal occlusion were included. This is so far the largest series of patients with ADAPT system. The complete recanalization rate was 84% with ADAPT versus 68% with stent retriever (P = 0.006). Unpublished data, Oral presentation at the European Stroke Organization, April 2015). Our research aims to show that a first line strategy of recanalization by thrombectomy using a distal suction system (ADAPT) is superior that the use of a stent retriever.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 381
• Est. completion date: February 2017
• Est. primary completion date: October 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age > 18 years with no upper age limit.

• Cerebral infarction in the anterior circulation

• Occlusion of the anterior circulation proven by CT angiography or MR angiography

• With or without previous Intravenous thrombolysis

• Start of thrombectomy procedure within 6 hours of symptoms onset.

• Patient expresses verbally his non-opposition to be enrolled in the study ; in case patient cannot communicate, verbal non-opposition is obtained from his close / trusted person

Exclusion Criteria:

• Absence of indication for thrombectomy

• Cons-indication for thrombectomy

• Presence of cerebral infarction of the posterior circulation

• Occlusion of the cervical carotid artery

• Allergy to x-ray contrast products

• Patient was bedridden or using a wheelchair most of the day (pre-event modified Rankin Scale score > 3) prior to stroke

• Pregnancy or breastfeeding

• Patient under legal protection

• No affiliation to health insurance

Secondary exclusion criteria

• Lack of access route for catheterization

Related Conditions & MeSH terms

• Cerebral Infarction
• Ischemia
• Ischemic Cerebrovascular Accident
• Stroke

Intervention

Procedure:
• direct aspiration procedure
Revascularization by endovascular thrombectomy using the distal aspiration first pass technique
• stent retriever procedure
Revascularization by endovascular thrombectomy using a mechanical thrombectomy device

Locations

Country	Name	City	State
France	CHU Pellegrin	Bordeaux
France	Hospices Civils de Lyon	Bron
France	CHU Dupuytren	Limoges
France	CHU Hôpital Gui de Chaulac	Montpellier
France	Hôpital Neurologique	Nancy
France	Hôpital Guillaume et René LAENNEC	Nantes
France	Fondation Ophtalmologique Adolphe de Rothschild	Paris
France	Hôpital Foch	Suresnes

Sponsors (1)

Lead Sponsor	Collaborator
Fondation Ophtalmologique Adolphe de Rothschild

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Complete recanalization percentage	Proportion of patients in which complete recanalization is achieved as defined by a TICI score equal to 2b or 3	Immediately after the revascularization procedure is completed