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Recruiting Phase 2

Head Down Tilt 15° to Increase Collateral Flow in Acute Ischemic Stroke

NCT06297863 · tracked via the Priya Life Science Italy tracker
Phase
Phase 2
Started
2025-03-01
Last updated
2026-05-06

Condition(s) studied

Acute Ischemic Stroke

Investigational drug(s) / intervention(s)

HEAD DOWN TILT -10° to -15°

HEAD DOWN TILT -10° to -15°: Head down tilt -10° to -15° (HDT15) is a positional therapy consisting of tilting the patient with the head -10° to -15° degrees below the rest of the body. Application of HDT15 will not delay usual care. The standard in-hospital patient pathway, including transfer from neuroimaging room to the angiography suite and the required procedural steps of MT, will allow sufficient time for the application of HDT15. HDT15 duration is expected to be at least 30 minutes (estimated time 30 to 90 minutes), from start to the assessment of the primary efficacy endpoint. The actual degree of HDT15 will be a range between -10° to -15°, depending on the angiographic system of each clinical site, but it will be maintained at -15° during the Emergency Room phase which is expected to account for \>50% of the total application time.

Study summary

The DOWN-SUITE study is multicenter, randomised, controlled, open-label clinical trial with blinded outcome assessment comparing collateral status in patients with acute ischemic stroke treated with an in-hospital application of head down tilt -10° to -15° (HDT15) versus usual positioning (0° to +30°) before endovascular mechanical thrombectomy.

This study will involve adult patients who are eligible for mechanical thrombectomy and who have acute ischemic stroke due to left or right middle cerebral artery occlusion (M1 segment).

The investigators hypothesise that HDT15, applied in acute ischemic stroke patients with a large vessel occlusion, will improve collateral circulation, prolong the survival of the ischemic penumbra and improve the clinical benefit from mechanical thrombectomy compared with standard of care (usual positioning 0° to +30°).

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Acute ischemic stroke due to left or right MCA occlusion of the M1 segment (excluding occlusion of the internal carotid artery terminus + M1) * Decision to treat with mechanical thrombectomy (with or without intravenous thrombolysis) * Informed consent obtained from patient or patient's next of kin, or emergency consent procedure Exclusion Criteria: * Impaired consciousness, defined as NIHSS score of 2 or 3 of the item 1a (level of consciousness): not alert, requires repeated stimulation or unresponsive. * Vomiting upon stroke onset. * History of glaucoma. * History or imaging findings of intracranial hypertension of any aetiology * Major breath disorders, defined as follows: * oxygen saturation ≤92% in room air at admission * severe chronic obstructive pulmonary disease (COPD) treated with long-term oxygen therapy. * severe heart failure with NYHA class 3 or 4 (breathlessness during ordinary physical activity or at rest). * Severe obesity, defined as body mass index (BMI) \> 35. * Patients participating in another interventional trial that would interfere with this study. * Female patients who are pregnant

Primary outcome measure(s)

  • Good collateral status — Day 0 (during mechanical thrombectomy)
    The primary endpoint will be the achievement of good collateral status, i.e. grade 3 or 4 on the American Society of Interventional and Therapeutic Neuroradiology/Society of Interventional Radiology (ASITN/SIR) collateral scale, in the HDT15 versus control group, as seen at the beginning of MT.15 The ASITN/SIR collateral grade will be assessed by a blinded central imaging core lab from the pretreatment diagnostic angiographic runs, routinely performed as the first procedural step of MT.

Trial sites (6)

FacilityCityRegionStatus
Ospedale Civile SS. Nicola e Filippo Avezzano Pronto Soccorso Avezzano Italy Not Yet Recruiting
Azienda Ospedaliero Universitaria Careggi Florence Italy Not Yet Recruiting
Azienda Ospedaliera Policlinico Universitario "G. Martino" Messina Italy Not Yet Recruiting
Fondazione IRCCS San Gerardo dei Tintori Monza Monza Italy Recruiting
Azienda Ospedaliero Universitaria Policlinico Umberto I Roma Italy Not Yet Recruiting
Ospedale Santa Maria della Misericordia Udine Italy Not Yet Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06297863 on ClinicalTrials.gov ↗ ← All trials in Italy