Thrombectomy Clinical Trials

Clinical trials related to Thrombectomy Procedure

A Pragmatic, Multicentre, Adaptive, Prospective, Open-label, Blinded Endpoint Randomized Clinical Trial Assessing the Impact of Head-of-bed Positioning at 0-degrees Versus 30-degrees or More on Functional Recovery Following Endovascular Thrombectomy for Anterior Circulation Large Vessel Occlusion Stroke.

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Endovascular thrombectomy (EVT), also known as clot retrieval, is a procedure that improves recovery for people who suffer a stroke by removing blood clots from large blood vessels in the brain. However, half of the patients undergoing EVT to remove the clot from a brain vessel still face lasting disabilities or even die within three months. The investigators of the HoBIT trial are trying to find out if the position of the head of bed improves recovery in patients who undergo EVT after suffering from a stroke. The purpose of this study is to establish the benefit of head of bed positioning at 0-degrees compared with 30-degrees or more after EVT for improving functional outcomes in adults that suffer from a stroke.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age 18 years or older on the date of randomization

• Endovascular thrombectomy (EVT) for large vessel occlusion (LVO) in the anterior circulation, according to current guidelines and local standards of clinical care. The definition of LVO may include the intracranial segment of the internal carotid artery (ICA), and/ or the M1 segment (proximal, mid, distal) of the middle cerebral artery (M1-MCA), and/ or the proximal M2 segment of the MCA (M2-MCA)

• Capable of giving signed informed consent either independently, or by a legally authorized representative (LAR), or via a deferred consent process approved by the relevant ethics committee, which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol.

Locations
Other Locations
Canada
Health Sciences North
RECRUITING
Greater Sudbury
Hamilton General Hospital
RECRUITING
Hamilton
Contact Information
Primary
Samantha Block, BSc
hobit@phri.ca
905-521-2100
Backup
Amanda Taylor, BSc
hobit@phri.ca
905-521-2100
Time Frame
Start Date: 2026-09-03
Estimated Completion Date: 2029-05
Participants
Target number of participants: 2240
Treatments
Experimental: Intervention Arm
Head of bed position of 0-degrees
Other: Control Arm
Head of bed position of 30-degrees or greater
Related Therapeutic Areas
Sponsors
Leads: Population Health Research Institute

This content was sourced from clinicaltrials.gov