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NCT06956521RecruitingPhase 1

Intra-Arterial Magnesium Therapy After Mechanical Thrombectomy in Acute Ischemic Stroke

Source: ClinicalTrials.gov · Last updated 1 Oct 2026

Brief summary (registry, in English)

The goal of this Phase I unblinded, dose-escalation trial is to evaluate the safety and tolerability of intra-arterial magnesium sulfate injection after mechanical thrombectomy in patients experiencing acute ischemic stroke. This trial is one of the first trials to look at IA administration of magnesium sulfate into at risk brain tissue in a selective and localized fashion.

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
30 (estimated)
First submitted
2 Dec 2024
Start date
1 Jul 2026
Primary completion date
Jul 2027
Lead sponsor
Baylor College of Medicine
Diseases
Stroke
NCT number
NCT06956521

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 30
  • From 1 Jul 2026 to the primary completion date, Jul 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • mRS\>2 caused by a history of prior stroke,
  • Unsuitable for this clinical study assessed by researcher. Subjects will not be excluded if they received IV t-PA as standard of care.

Other illness

  • subjects on therapeutic anticoagulation, as it is a relative contraindication to MT, and could be a confounding variable predisposing to intracranial hemorrhage including coagulation disorders, systematic hemorrhagic tendency, thrombocytopenia \<80000/mm3;
  • Second or third-degree heart block without a pacemaker in place,
  • patients taking digoxin or other cardiac glycoside

Lab values

  • Patient already enrolled in another experimental treatment trial. Exclusion criteria 1-3 are all contraindications to magnesium therapy,
  • Severe hepatic dysfunction, severe renal dysfunction (\<30 mL/min), increase in ALT or AST (more than 2 times of upper limit of normal value), increase in serum creatinine (more than 1.5 times of upper limit of normal value) or requiring dialysis;

Other

  • Positive pregnancy test;
  • those undergoing MT with a TICI \<2a revascularization;
  • tandem occlusion of the cervical common or internal carotid artery; and
  • Technical inability to navigate micro-catheter to target clot,
  • patient is on neuromuscular blocking agents including depolarizing (succinylcholine) and nondepolarizing subtypes (rocuronium, vecuronium, etc);
  • patient is taking any form of CNS depressant including barbiturates, narcotics, outside the setting of anesthesia or ICU sedation

Who the study is looking for

  • Patient with acute cerebral ischemia due to ICA or MCA occlusion
  • Major neurologic deficits: 6≤NIHSS≤20,
  • Premorbid mRS 0 or 1, or 2
  • Patient's clinical attending physician plans MT procedure as part of routine clinical care,
  • undergo MT with a TICI 2a or better recanalization,
  • Signed informed consent.

Age in the registry: 21 years to 95 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Baylor St. Luke's Medical Center
Coordinator of this site? Confirm its status
HoustonUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.