Clinical trial Recruiting at 1 site Phase 2 Interventional Ages 18 and up

Moderate CO2 increase during anesthesia to boost collateral flow in clot removal for acute anterior stroke

Official title: Evaluation of the Effect of Moderate and Controlled Hypercapnia on Ischemic Penumbra Vascular Collaterality During General Anesthesia for Anterior Circulation Acute Ischemic Stroke Mechanical Thrombectomy

Run by University Hospital, Clermont-Ferrand · NCT05051397 · Data updated 2026-11-12

This study will test whether slightly higher blood carbon dioxide during anesthesia improves collateral blood flow and protects the brain in people having mechanical thrombectomy for anterior large-vessel ischemic stroke.

Quick facts

PhasePhase 2
Study typeInterventional
Ages18 Years and up
SexAll
Enrollment50 (estimated)
SponsorUniversity Hospital, Clermont-Ferrand
Academic / other
Locations1 site (Clermont-Ferrand)
StatusRecruiting
StartedJuly 20, 2022
Main results expectedOctober 20, 2028
Study endsOctober 20, 2028
Registry record updatedSeptember 3, 2026
Trial IDNCT05051397 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults with anterior-circulation large-vessel occlusion ischemic stroke who are eligible for mechanical thrombectomy under general anesthesia and meet the trial's inclusion/exclusion criteria.

Probably not a fit

Patients with active smoking, chronic respiratory failure, BMI over 40, prior intubation, suspected elevated intracranial pressure, pregnancy, or posterior-circulation strokes are excluded and likely would not benefit from this approach.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized Phase 2 trial enrolls patients with anterior-circulation large-vessel occlusion ischemic stroke who undergo mechanical thrombectomy under general anesthesia. After induction and intubation, patients are randomized to moderate hypercapnia (target PaCO2 50 mmHg) or normocapnia (target PaCO2 40 mmHg) achieved by adjusting ventilator settings with arterial blood gas confirmation. Baseline and pre-reperfusion collateral circulation will be graded using the ASITN scale on angiography while systolic blood pressure and anesthetic depth are standardized. The study compares the effect of controlled CO2 modulation on collateral blood flow and periprocedural cerebral protection prior to intra-arterial revascularization.

Why it matters

Potential benefit: If successful, moderate hypercapnia during anesthesia could increase collateral cerebral blood flow before reperfusion and reduce ischemic injury, potentially improving recovery after thrombectomy.

How similar studies have gone: Physiologic and observational studies show hypercapnia increases cerebral blood flow, but randomized evidence testing CO2 modulation specifically during thrombectomy is limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

• Large vessel occlusion anterior circulation stroke (terminal carotid artery and/or middle cerebral artery M1-M2 segment) eligible to mechanical thrombectomy under general anesthesia

Exclusion Criteria :

* Active smoker
* Chronic respiratory failure with ambulatory oxygen supplementation
* Obesity with BMI\>40Kg/ m2
* Intubation before the procedure
* Heart failure with intolerance to decubitus
* Severe renal failure
* Suspected elevated intracranial pressure
* Pregnant or breastfeeding women

Where it's running

  • Chu
    Clermont-Ferrand, France
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.